Canonical Allele Identifier: PA2741935548
Gene: SLC19A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2615475
ClinVar RCV Id: RCV003367445
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008927.1:p.Asp2Glu
CA343112671
NM_006996.3:c.6T>G
CA343112673
NM_006996.3:c.6T>A