Canonical Allele Identifier: PA915978039
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 8594
ClinVar RCV Id: RCV000009125
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119580.2:p.Gly630Val
CA119778
NM_001126108.2:c.1889G>T