Canonical Allele Identifier: PA215799
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 41723

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Glu11Gln
CA000106
NM_001126114.3:c.31G>C