Canonical Allele Identifier: PA2829320175
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3165721
ClinVar RCV Id: RCV004457051

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387841.1:p.Ala161Ser
CA414749952
NM_001400912.1:c.481G>T