Canonical Allele Identifier: PA2828375039
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1056779
ClinVar RCV Id: RCV001365658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357014.1:p.Phe354Leu
CA407962530
NM_001370085.1:c.1062C>G
CA407962531
NM_001370085.1:c.1062C>A
CA407962536
NM_001370085.1:c.1060T>C