Canonical Allele Identifier: PA915961038
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 225470
ClinVar RCV Id: RCV000490297 RCV000713330
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000330.3:p.Leu858His
CA8069962
NM_000339.3:c.2573T>A