Canonical Allele Identifier: PA2826362089
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 549671
ClinVar RCV Id: RCV000664211 RCV002440408
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240745.1:p.Trp99Cys
CA4938159
NM_001253816.2:c.297G>C
CA372626736
NM_001253816.2:c.297G>T