Canonical Allele Identifier: PA2826566498
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 950660
ClinVar RCV Id: RCV001222415 RCV002411820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Asp22Gly
CA397846192
NM_001276761.3:c.65A>G