Canonical Allele Identifier: PA117728
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_055085.1:p.Gly259Arg
CA117727
NM_014270.5:c.775G>A
CA405201975
NM_014270.5:c.775G>C