Canonical Allele Identifier: PA645420018
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 429719
ClinVar RCV Id: RCV000494259

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006350.1:p.Gly41Glu
CA10524594
NM_006359.3:c.122G>A