Canonical Allele Identifier: PA2825616390
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2450758
ClinVar RCV Id: RCV003177183

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Asp192Glu
CA397835829
NM_001126117.1:c.576T>A
CA397835833
NM_001126117.1:c.576T>G