Canonical Allele Identifier: PA1139726702
Gene: SLC7A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 933266
ClinVar RCV Id: RCV001201441 RCV002504227
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055085.1:p.Asn271Ser
CA9358626
NM_014270.5:c.812A>G