Canonical Allele Identifier: PA658829874
Gene: CSNK1D HGNC NCBI

Linked Data

ClinVar Variation Id: 8741
ClinVar RCV Id: RCV000009280

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620693.1:p.Thr44Ala
CA119878
NM_139062.4:c.130A>G