Canonical Allele Identifier: PA117722
Gene: SLC7A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 5780
ClinVar RCV Id: RCV000006136
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055085.1:p.Val170Met
CA117721
NM_014270.5:c.508G>A