Allele Registry

Canonical Allele Identifier: PA264791

Gene: KCND3 HGNC NCBI

ClinVar RCV:

RCV000056298

RCV001268494

ClinVar Variation:

66061

HGVS (amino-acid)	Matching Registered Transcripts
NP_004971.2:p.Phe227del	CA264789 NM_004980.5:c.680_682del