Allele Registry

Canonical Allele Identifier: PA2827264441

Gene: TP63 HGNC NCBI

ClinVar RCV:

RCV000494181

ClinVar Variation:

430080

HGVS (amino-acid)	Matching Registered Transcripts
NP_001316074.1:p.Gly79Val	CA355750729 NM_001329145.2:c.236G>T