Canonical Allele Identifier: PA2826395239
Gene: SLC12A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1679711
ClinVar RCV Id: RCV002227735 RCV003093902
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243390.1:p.Ala1173Val
CA3393738
NM_001256461.2:c.3518C>T