Canonical Allele Identifier: PA169190
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Thr304Ala
CA000493
NM_001126112.3:c.910A>G