Canonical Allele Identifier: PA658828100
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 546135

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006350.1:p.Ala96Pro
CA414606922
NM_006359.3:c.286G>C