Allele Registry

Canonical Allele Identifier: PA279675

Gene: SLC12A5 HGNC NCBI

ClinVar RCV:

RCV000202007

ClinVar Variation:

217905

HGVS (amino-acid)	Matching Registered Transcripts
NP_001128243.1:p.Gly551Asp	CA279674 NM_001134771.2:c.1652G>A