Canonical Allele Identifier: PA2828374959
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1044232
ClinVar RCV Id: RCV001348455 RCV002395771
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357014.1:p.Leu255Phe
CA407963147
NM_001370085.1:c.763C>T