Canonical Allele Identifier: PA645390180
Gene: SLC7A7 HGNC NCBI

Linked Data

ClinVar Variation Id: 312815

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119578.1:p.Glu376Asp
CA7104471
NM_001126106.4:c.1128A>C
CA388922636
NM_001126106.4:c.1128A>T