Canonical Allele Identifier: PA2828077496
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 540430
ClinVar RCV Id: RCV000650460
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350051.1:p.Met259Val
CA4938452
NM_001363122.2:c.775A>G