Canonical Allele Identifier: PA2827340509
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 197277
ClinVar RCV Id: RCV000178269

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317581.1:p.Phe120Val
CA245318
NM_001330652.2:c.358T>G