Canonical Allele Identifier: PA891857372
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 572609
ClinVar RCV Id: RCV000694032
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006350.1:p.Arg3Leu
CA336084215
NM_006359.3:c.8G>T