Canonical Allele Identifier: PA658810349
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 521445
ClinVar RCV Id: RCV000623631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005651.1:p.Gly273Asp
CA412895151
NM_005660.3:c.818G>A