Canonical Allele Identifier: PA2828076156
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 664998
ClinVar RCV Id: RCV000823198
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350047.1:p.Leu94Val
CA372626680
NM_001363118.2:c.280C>G