Canonical Allele Identifier: PA318517
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 207238

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001036002.1:p.Arg202Gly
CA318515
NM_001042537.2:c.604A>G