Allele Registry

Canonical Allele Identifier: PA2829948165

Gene: SLC12A5 HGNC NCBI

ClinVar RCV:

RCV000202007

ClinVar Variation:

217905

HGVS (amino-acid)	Matching Registered Transcripts
NP_065759.1:p.Gly528Asp	CA279674 NM_020708.5:c.1583G>A