Canonical Allele Identifier: PA2827036829
Gene: SLC19A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 917418
ClinVar RCV Id: RCV001174381 RCV002559674
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001306596.1:p.Pro33Gln
CA343112308
NM_001319667.1:c.98C>A