Canonical Allele Identifier: PA645376275
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 429375
ClinVar RCV Id: RCV000494168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_212134.3:p.Leu445Arg
CA9724518
NM_033409.4:c.1334T>G