Canonical Allele Identifier: PA169752
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142916

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Asn131Asp
CA000419
NM_001126116.1:c.391A>G