Canonical Allele Identifier: PA169756
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142916

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Asn263Asp
CA000419
NM_001126112.3:c.787A>G