Canonical Allele Identifier: PA347002
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 210032
ClinVar RCV Id: RCV000191977 RCV001195405
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_212134.3:p.Arg212Cys
CA347001
NM_033409.4:c.634C>T