Canonical Allele Identifier: PA2826566766
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 482230

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Pro113Ser
CA002580
NM_001276761.3:c.337C>T