Canonical Allele Identifier: PA1139676988
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 992415
ClinVar RCV Id: RCV001280858 RCV003235535
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119580.2:p.Cys416Ser
CA395985818
NM_001126108.2:c.1246T>A
CA395985828
NM_001126108.2:c.1247G>C