Canonical Allele Identifier: PA2825601799
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2036477
ClinVar RCV Id: RCV002899177

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Leu299Pro
CA397836397
NM_001126112.3:c.896T>C