Canonical Allele Identifier: PA916074909
Gene: CSNK2A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 421395
ClinVar RCV Id: RCV000479609 RCV001249615
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_808228.1:p.Asp20Glu
CA16620934
NM_177560.3:c.60T>A
CA407933096
NM_177560.3:c.60T>G