Canonical Allele Identifier: PA345439
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 96703
ClinVar RCV Id: RCV000082865
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240744.1:p.Tyr305Cys
CA345438
NM_001253815.2:c.914A>G