Canonical Allele Identifier: PA2827036850
Gene: SLC19A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2169485
ClinVar RCV Id: RCV003084851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001306596.1:p.Leu64Pro
CA343112093
NM_001319667.1:c.191T>C