Allele Registry

Canonical Allele Identifier: PA2828109775

Gene: CSNK1D HGNC NCBI

ClinVar RCV:

RCV000009280

ClinVar Variation:

8741

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350678.1:p.Thr44Ala	CA119878 NM_001363749.2:c.130A>G