Canonical Allele Identifier: PA658802038
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 512592

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001036002.1:p.Val225Ile
CA10524682
NM_001042537.2:c.673G>A