Canonical Allele Identifier: PA318537
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 207247

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006350.1:p.Ala50Ser
CA318535
NM_006359.3:c.148G>T