Canonical Allele Identifier: PA2828076190
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1517510
ClinVar RCV Id: RCV002041103
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350047.1:p.Pro134Ser
CA372627077
NM_001363118.2:c.400C>T