Canonical Allele Identifier: PA645429662
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 245818
ClinVar RCV Id: RCV000237012
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078807.1:p.Val36Gly
CA10584287
NM_024531.5:c.107T>G