Canonical Allele Identifier: PA117732
Gene: SLC7A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 5788
ClinVar RCV Id: RCV000006144
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055085.1:p.Ile44Thr
CA117731
NM_014270.5:c.131T>C