Allele Registry

Canonical Allele Identifier: PA915995913

Gene: SLC12A1 HGNC NCBI

ClinVar RCV:

RCV000009296

ClinVar Variation:

8753

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171761.1:p.Val272Phe	CA119889 NM_001184832.2:c.814G>T