Canonical Allele Identifier: PA2829948499
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_065759.1:p.Ser1034Ile
CA9887781
NM_020708.5:c.3101G>T