Canonical Allele Identifier: PA2579951736
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2679228
ClinVar RCV Id: RCV003464698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Pro322Arg
CA397835872
NM_000546.6:c.965C>G