Canonical Allele Identifier: PA2829320015
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1700560
ClinVar RCV Id: RCV002274809

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387839.1:p.Phe384Leu
CA414752906
NM_001400910.1:c.1150T>C
CA414752920
NM_001400910.1:c.1152C>G
CA414752923
NM_001400910.1:c.1152C>A