Canonical Allele Identifier: PA339072
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 216466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119585.1:p.Leu130Phe
CA339065
NM_001126113.3:c.388C>T