Canonical Allele Identifier: PA102465
Gene: SLC7A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 5783
ClinVar RCV Id: RCV000006139
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119807.1:p.Gly195Arg
CA117725
NM_001126335.2:c.583G>A
CA405202749
NM_001126335.2:c.583G>C