Canonical Allele Identifier: PA2826567695
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2578516
ClinVar RCV Id: RCV003326292

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Asp285Asn
CA397835847
NM_001276761.3:c.853G>A