Canonical Allele Identifier: PA2826662152
Gene: SLC35A2 HGNC NCBI
ClinVar Allele:
59490
ClinVar RCV:
RCV000043516
ClinVar Variation:
50365
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269580.1:p.Met1Ile