Canonical Allele Identifier: PA2827264546
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6532

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316074.1:p.Arg225Cys
CA118338
NM_001329145.2:c.673C>T