Canonical Allele Identifier: PA211246
Gene: SLC7A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 5782
ClinVar RCV Id: RCV000006138 RCV000480556 RCV004018572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055085.1:p.Ala182Thr
CA211245
NM_014270.5:c.544G>A