Canonical Allele Identifier: PA2829320064
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1705001
ClinVar RCV Id: RCV002283328

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387840.1:p.Ser19Gly
CA414606761
NM_001400911.1:c.55A>G