Canonical Allele Identifier: PA2828165230
Gene: SLC12A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 521402
ClinVar RCV Id: RCV000623060 RCV002287895 RCV002532836
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352017.1:p.Arg207His
CA391612748
NM_001365088.1:c.620G>A