Canonical Allele Identifier: PA2828109775
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_001350678.1:p.Thr44Ala
CA119878
NM_001363749.2:c.130A>G