Canonical Allele Identifier: PA2825596698
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1490589
ClinVar RCV Id: RCV001983815

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119579.2:p.Leu858Phe
CA395997333
NM_001126107.2:c.2572C>T