Canonical Allele Identifier: PA2828375234
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1992208
ClinVar RCV Id: RCV002814319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357015.1:p.Gly146Arg
CA407963837
NM_001370086.1:c.436G>C
CA407963838
NM_001370086.1:c.436G>A