Canonical Allele Identifier: PA346970
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 210012
ClinVar RCV Id: RCV000191957 RCV000790977 RCV001589066 RCV002362997 RCV003417696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_212134.3:p.Asn21Ser
CA346969
NM_033409.4:c.62A>G