Canonical Allele Identifier: PA2826662034
Gene: SLC35A2 HGNC NCBI
ClinVar RCV:
RCV000414069
ClinVar Variation:
373073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269579.1:p.Ser226del
CA16043321
NM_001282650.2:c.676_678del