Canonical Allele Identifier: PA2825409198
Gene: SLC12A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1424771
ClinVar RCV Id: RCV001957250 RCV002560471
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035961.1:p.Trp201Cys
CA391612685
NM_001042496.2:c.603G>T
CA391612688
NM_001042496.2:c.603G>C