Canonical Allele Identifier: PA645436261
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376650

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Arg81Leu
CA16603067
NM_001126117.1:c.242G>T