Canonical Allele Identifier: PA102630
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_001119807.1:p.Val170Met
CA117721
NM_001126335.2:c.508G>A