Canonical Allele Identifier: PA645466158
Gene: SLC35A2 HGNC NCBI
ClinVar RCV:
RCV000414069
ClinVar Variation:
373073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005651.1:p.Ser213del
CA16043321
NM_005660.3:c.637_639del