Canonical Allele Identifier: PA2825619078
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 230382

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Pro277Thr
CA001212
NM_001126118.1:c.829C>A