Allele Registry

Canonical Allele Identifier: PA915995914

Gene: SLC12A1 HGNC NCBI

ClinVar RCV:

RCV000256371

ClinVar Variation:

265983

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171761.1:p.Glu281Asp	CA10588934 NM_001184832.2:c.843G>C CA392307224 NM_001184832.2:c.843G>T