Canonical Allele Identifier: PA658804206
Gene: CLCNKB HGNC NCBI

Linked Data

ClinVar Variation Id: 504916
ClinVar RCV Id: RCV000606374 RCV000986251 RCV001653945 RCV001578909
ClinVar Variation Id: 789426
ClinVar RCV Id: RCV000972058 RCV002503081
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000076.2:p.Ala214Gly
CA623400
NM_000085.5:c.641C>G
CA18332661
NM_000085.5:c.641_642delinsGC