Canonical Allele Identifier: PA2826314486
Gene: SLC7A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 770656
ClinVar RCV Id: RCV000949840

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229965.1:p.Ala214Thr
CA9358736
NM_001243036.2:c.640G>A