Canonical Allele Identifier: PA2826314562
Gene: SLC7A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 889688
ClinVar RCV Id: RCV001123747 RCV001216402 RCV003396758
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229965.1:p.Tyr457His
CA9358429
NM_001243036.2:c.1369T>C