Canonical Allele Identifier: PA168216
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Val34Met
CA000075
NM_001126118.1:c.100G>A