Canonical Allele Identifier: PA645376218
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 262239
ClinVar RCV Id: RCV000245544 RCV001516819 RCV001610741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_212134.3:p.Pro267Leu
CA9724680
NM_033409.4:c.800C>T