Canonical Allele Identifier: PA916074900
Gene: CSNK2A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 619014
ClinVar RCV Id: RCV000757921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_808228.1:p.Asp20His
CA407933108
NM_177560.3:c.58G>C