Canonical Allele Identifier: PA106257
Gene: SLC7A14 HGNC NCBI

Linked Data

ClinVar Variation Id: 126446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066000.2:p.Gly330Arg
CA151150
NM_020949.3:c.988G>A
CA355492064
NM_020949.3:c.988G>C