Canonical Allele Identifier: PA2825143116
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 8592

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000330.3:p.Pro349Leu
CA119776
NM_000339.3:c.1046C>T