Canonical Allele Identifier: PA2825142821
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 101514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000330.3:p.Thr60Met
CA150734
NM_000339.3:c.179C>T