Canonical Allele Identifier: PA2499275526
Gene: SLC19A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1034343
ClinVar RCV Id: RCV001337041
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008927.1:p.Phe42Val
CA343112236
NM_006996.3:c.124T>G