Canonical Allele Identifier: PA169755
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142916

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Asn263Asp
CA000419
NM_000546.6:c.787A>G