Canonical Allele Identifier: PA318508
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 207235
ClinVar RCV Id: RCV000189403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001036002.1:p.Arg23Gly
CA318507
NM_001042537.2:c.67A>G