Canonical Allele Identifier: PA2825601679
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 458572
ClinVar RCV Id: RCV000535005

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Arg290Pro
CA397836589
NM_001126112.3:c.869G>C