Canonical Allele Identifier: PA2580340990
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1705001
ClinVar RCV Id: RCV002283328

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006350.1:p.Ser71Gly
CA414606761
NM_006359.3:c.211A>G