Canonical Allele Identifier: PA2825601659
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2119726
ClinVar RCV Id: RCV003033239

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Asn288Thr
CA397836634
NM_001126112.3:c.863A>C