Canonical Allele Identifier: PA1139726715
Gene: SLC7A9 HGNC NCBI
ClinVar RCV:
RCV001236154
ClinVar Variation:
962317
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055085.1:p.Glu282Lys
CA9358616
NM_014270.5:c.844G>A