Canonical Allele Identifier: PA2826361869
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3165182
ClinVar RCV Id: RCV004464033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240744.1:p.Val293Met
CA372628199
NM_001253815.2:c.877G>A