ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579936038
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.6708604299
Score
-0.072442842
Score
1.2860517474
Score
-0.7151991708
Linked Data - NCBI & NCI
ClinVar Allele:
363559
ClinVar RCV:
RCV000417511
RCV000418221
RCV000418859
RCV000423239
RCV000423893
RCV000425645
RCV000428451
RCV000431265
RCV000434193
RCV000435900
RCV000436639
RCV000438678
RCV000440924
RCV000441609
RCV001023195
RCV001071488
RCV002289543
RCV003476012
ClinVar Variation:
376680
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Tyr163His
CA16603094
NM_000546.6:c.487T>C