Allele Registry

Canonical Allele Identifier: PA915961033

Gene: SLC12A3 HGNC NCBI

ClinVar Allele:

480535

ClinVar RCV:

RCV000576426

RCV002526929

ClinVar Variation:

487479

HGVS (amino-acid)	Matching Registered Transcripts
NP_000330.3:p.Asp841Gly	CA395996336 NM_000339.3:c.2522A>G