Canonical Allele Identifier: PA915978061
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 8588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119580.2:p.Arg655His
CA119770
NM_001126108.2:c.1964G>A