Canonical Allele Identifier: PA645390056
Gene: SLC7A7 HGNC NCBI

Linked Data

ClinVar Variation Id: 380186

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119578.1:p.Ala91Val
CA7104737
NM_001126106.4:c.272C>T