Canonical Allele Identifier: PA2580157137
Gene: SLC12A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2319018
ClinVar RCV Id: RCV004166146
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128243.1:p.Ser1057Ile
CA9887781
NM_001134771.2:c.3170G>T