Allele Registry

Canonical Allele Identifier: PA2825143053

Gene: SLC12A3 HGNC NCBI

ClinVar Allele:

205781

ClinVar RCV:

RCV000191129

RCV000681951

ClinVar Variation:

209191

HGVS (amino-acid)	Matching Registered Transcripts
NP_000330.3:p.Leu272Pro	CA250393 NM_000339.3:c.815T>C