Canonical Allele Identifier: PA2830247398
Gene: SLC12A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 450842
ClinVar RCV Id: RCV000522664 RCV001829501
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_598408.1:p.Gly125Val
CA7464582
NM_133647.2:c.374G>T