Canonical Allele Identifier: PA2826562614
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2036477
ClinVar RCV Id: RCV002899177

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Leu140Pro
CA397836397
NM_001276697.3:c.419T>C