Canonical Allele Identifier: PA101612
Gene: SLC7A7 HGNC NCBI

Linked Data

ClinVar Variation Id: 56371
ClinVar RCV Id: RCV000049784

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119577.1:p.Thr188Ile
CA263825
NM_001126105.3:c.563C>T