Canonical Allele Identifier: PA145449
Gene: SLC35A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 89030
ClinVar RCV Id: RCV000074504 RCV001588895
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036375.1:p.Ser296Gly
CA145448
NM_012243.2:c.886A>G