Canonical Allele Identifier: PA117724
Gene: SLC7A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 5781
ClinVar RCV Id: RCV000006137 RCV000523825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055085.1:p.Gly105Arg
CA117723
NM_014270.5:c.313G>A
CA405203860
NM_014270.5:c.313G>C