Canonical Allele Identifier: PA2826314461
Gene: SLC7A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 5780
ClinVar RCV Id: RCV000006136

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229965.1:p.Val170Met
CA117721
NM_001243036.2:c.508G>A