Canonical Allele Identifier: PA2825408436
Gene: SLC12A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2081244
ClinVar RCV Id: RCV002994134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035960.1:p.Leu159Pro
CA7464526
NM_001042495.2:c.476T>C