Allele Registry

Canonical Allele Identifier: PA2826202828

Gene: SLC12A8 HGNC NCBI

ClinVar RCV:

RCV004103211

ClinVar Variation:

2240261

HGVS (amino-acid)	Matching Registered Transcripts
NP_001182412.2:p.Val106Phe	CA354287766 NM_001195483.2:c.316G>T