Canonical Allele Identifier: PA102476
Gene: SLC7A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 5784
ClinVar RCV Id: RCV000006140 RCV000793254
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119807.1:p.Gly259Arg
CA117727
NM_001126335.2:c.775G>A
CA405201975
NM_001126335.2:c.775G>C