Canonical Allele Identifier: PA2573252917
Gene: SLC19A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1379000
ClinVar RCV Id: RCV001883544
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008927.1:p.Arg26His
CA343112404
NM_006996.3:c.77G>A