Canonical Allele Identifier: PA2828375083
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1463783
ClinVar RCV Id: RCV001975291
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357014.1:p.Ser411Arg
CA407962059
NM_001370085.1:c.1233T>A
CA407962060
NM_001370085.1:c.1233T>G
CA407962066
NM_001370085.1:c.1231A>C