Canonical Allele Identifier: PA2828808578
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3165721
ClinVar RCV Id: RCV004457051

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366039.1:p.Ala161Ser
CA414749952
NM_001379110.1:c.481G>T