Canonical Allele Identifier: PA2825411559
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1491650
ClinVar RCV Id: RCV001988798

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001036002.1:p.Arg20Gly
CA414606430
NM_001042537.2:c.58C>G