Canonical Allele Identifier: PA2826127037
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 469635
ClinVar RCV Id: RCV000533095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171122.1:p.Leu38Pro
CA414606885
NM_001177651.2:c.113T>C