Canonical Allele Identifier: PA2828808533
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1705001
ClinVar RCV Id: RCV002283328

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366039.1:p.Ser19Gly
CA414606761
NM_001379110.1:c.55A>G