Canonical Allele Identifier: PA1139752556
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 929820
ClinVar RCV Id: RCV001269384
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078807.1:p.Phe135del
CA848870182
NM_024531.5:c.405_407del