Canonical Allele Identifier: PA2826560232
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 100816
ClinVar RCV Id: RCV000087174

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.His257Arg
CA000476
NM_001276695.3:c.770A>G