Canonical Allele Identifier: PA2580340999
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1798016

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006350.1:p.Phe98Leu
CA414606935
NM_006359.3:c.292T>C
CA414606939
NM_006359.3:c.294C>A
CA414606940
NM_006359.3:c.294C>G