Canonical Allele Identifier: PA2826127091
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 512592
ClinVar RCV Id: RCV000871818 RCV002065336 RCV002358707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171122.1:p.Val173Ile
CA10524682
NM_001177651.2:c.517G>A