Canonical Allele Identifier: PA645436338
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 428892

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Glu92Ala
CA397839786
NM_001126117.1:c.275A>C