Canonical Allele Identifier: PA2826362117
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 655793
ClinVar RCV Id: RCV000812044 RCV002370185
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240745.1:p.Leu133Met
CA4938183
NM_001253816.2:c.397C>A