Canonical Allele Identifier: PA2826565601
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 265337
ClinVar RCV Id: RCV000255449 RCV000418361 RCV000427564 RCV000437324 RCV000439730 RCV000445278 RCV000429054 RCV000430142 RCV000436667 RCV000419408 RCV000700891 RCV000772138 RCV000785239 RCV002282093 RCV004021028
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Ser176Gly
CA10588671
NM_001276760.3:c.526A>G