Canonical Allele Identifier: PA2825612775
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 428883
ClinVar RCV Id: RCV000492745
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Val40Gly
CA397841550
NM_001126116.1:c.119T>G