ClinGen Allele Registry
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Canonical Allele Identifier:
PA287753
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.9346120435
Score
0.076833621
Score
-1.3053155287
Score
0.6722395765
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000115728
RCV000417813
RCV000418414
RCV000419908
RCV000421548
RCV000426684
RCV000428029
RCV000429595
RCV000434383
RCV000436065
RCV000439186
RCV000439843
RCV001377420
RCV002288598
RCV002288599
RCV003997297
ClinVar Variation:
127817
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Leu194Phe
CA000278
NM_000546.6:c.580C>T