Canonical Allele Identifier: PA101455
Gene: SLC7A7 HGNC NCBI

Linked Data

ClinVar Variation Id: 56367
ClinVar RCV Id: RCV000049780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119577.1:p.Ala140Pro
CA263815
NM_001126105.3:c.418G>C