Canonical Allele Identifier: PA2828808548
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1798016

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366039.1:p.Phe46Leu
CA414606935
NM_001379110.1:c.136T>C
CA414606939
NM_001379110.1:c.138C>A
CA414606940
NM_001379110.1:c.138C>G