Canonical Allele Identifier: PA2827264751
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6532

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316075.1:p.Arg140Cys
CA118338
NM_001329146.2:c.418C>T