Canonical Allele Identifier: PA2825142188
Gene: SLC12A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3162819
ClinVar RCV Id: RCV004456218
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000329.2:p.Tyr246Cys
CA7546892
NM_000338.3:c.737A>G