Canonical Allele Identifier: PA166963
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 141967

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Ala86Thr
CA000088
NM_001126112.3:c.256G>A