Allele Registry

Canonical Allele Identifier: PA279805

Gene: SLC12A5 HGNC NCBI

ClinVar RCV:

RCV000202258

ClinVar Variation:

217904

HGVS (amino-acid)	Matching Registered Transcripts
NP_001128243.1:p.Leu426Pro	CA279804 NM_001134771.2:c.1277T>C