Canonical Allele Identifier: PA100264
Gene: CSNK1D HGNC NCBI

Linked Data

ClinVar Variation Id: 8741
ClinVar RCV Id: RCV000009280
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001884.2:p.Thr44Ala
CA119878
NM_001893.6:c.130A>G