Canonical Allele Identifier: PA2826361856
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 956139
ClinVar RCV Id: RCV001228886 RCV002563153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240744.1:p.Arg275Cys
CA4938285
NM_001253815.2:c.823C>T