Allele Registry

Canonical Allele Identifier: PA658829877

Gene: CSNK1D HGNC NCBI

ClinVar RCV:

RCV000043507

ClinVar Variation:

50319

HGVS (amino-acid)	Matching Registered Transcripts
NP_620693.1:p.His46Arg	CA143736 NM_139062.4:c.137A>G