Canonical Allele Identifier: PA2573173139
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_001037.1:p.Ala1189Val
CA3393738
NM_001046.3:c.3566C>T