ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579936850
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.0233517767
Score
0.4631156797
Score
-0.0489664566
Score
-3.184903906
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000569462
RCV000633349
RCV002289789
RCV003492102
ClinVar Variation:
480743
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Pro128Thr
CA397843906
NM_000546.6:c.382C>A