Canonical Allele Identifier: PA645390136
Gene: SLC7A7 HGNC NCBI

Linked Data

ClinVar Variation Id: 312820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119578.1:p.Ile311Val
CA7104537
NM_001126106.4:c.931A>G