Canonical Allele Identifier: PA2828808537
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1878535
ClinVar RCV Id: RCV002510626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366039.1:p.Leu23Val
CA336084467
NM_001379110.1:c.67C>G