Canonical Allele Identifier: PA2573165795
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1490589
ClinVar RCV Id: RCV001983815

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000330.3:p.Leu859Phe
CA395997333
NM_000339.3:c.2575C>T