Canonical Allele Identifier: PA263814
Gene: SLC7A7 HGNC NCBI

Linked Data

ClinVar Variation Id: 56366
ClinVar RCV Id: RCV000049779 RCV001778694
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119578.1:p.Leu124Pro
CA263811
NM_001126106.4:c.371T>C