Canonical Allele Identifier: PA2499287312
Gene: SLC7A14 HGNC NCBI

Linked Data

ClinVar Variation Id: 1018162
ClinVar RCV Id: RCV001317423
ClinVar Variation Id: 1495193
ClinVar RCV Id: RCV002015209

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066000.2:p.Gly368Arg
CA2701716
NM_020949.3:c.1102G>A
CA2701717
NM_020949.3:c.1102G>C