Canonical Allele Identifier: PA2826314472
Gene: SLC7A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 5782
ClinVar RCV Id: RCV000006138 RCV000480556 RCV004018572
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229965.1:p.Ala182Thr
CA211245
NM_001243036.2:c.544G>A