Canonical Allele Identifier: PA915977853
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 635427
ClinVar RCV Id: RCV000786876

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119580.2:p.Leu170Pro
CA395980724
NM_001126108.2:c.509T>C