Canonical Allele Identifier: PA2825602880
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 950660

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119585.1:p.Asp61Gly
CA397846192
NM_001126113.3:c.182A>G