Canonical Allele Identifier: PA2828374907
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 476612
ClinVar RCV Id: RCV000550541 RCV002341461
ClinVar Variation Id: 852705
ClinVar RCV Id: RCV001057369
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357014.1:p.Ser175Arg
CA9724759
NM_001370085.1:c.525C>A
CA407963661
NM_001370085.1:c.525C>G
CA407963667
NM_001370085.1:c.523A>C