Canonical Allele Identifier: PA2828374787
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2683525
ClinVar RCV Id: RCV003480345
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357014.1:p.Val11Ala
CA407964683
NM_001370085.1:c.32T>C
CA2697547263
NM_001370085.1:c.32_33delinsCT