Canonical Allele Identifier: PA2826127083
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3165721
ClinVar RCV Id: RCV004457051

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171122.1:p.Ala161Ser
CA414749952
NM_001177651.2:c.481G>T