Canonical Allele Identifier: PA2828808586
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 512592

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366039.1:p.Val173Ile
CA10524682
NM_001379110.1:c.517G>A