Canonical Allele Identifier: PA2827265542
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 1070564

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316078.1:p.Gly242Asp
CA355755120
NM_001329149.2:c.725G>A