Canonical Allele Identifier: PA915977931
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 64413
ClinVar RCV Id: RCV000054600 RCV002515739 RCV002504952
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119580.2:p.Val397Met
CA216088
NM_001126108.2:c.1189G>A