Canonical Allele Identifier: PA192240
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12358
ClinVar Variation Id: 574679

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Val140Leu
CA000430
NM_001126116.1:c.418G>T
CA397837009
NM_001126116.1:c.418G>C