Canonical Allele Identifier: PA101621
Gene: SLC7A7 HGNC NCBI

Linked Data

ClinVar Variation Id: 56344
ClinVar RCV Id: RCV000049757

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119577.1:p.Thr5Ile
CA263748
NM_001126105.3:c.14C>T