Canonical Allele Identifier: PA339799
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 145
ClinVar RCV Id: RCV000000168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_212134.3:p.Pro28Thr
CA339798
NM_033409.4:c.82C>A