Canonical Allele Identifier: PA2826662152
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50365
ClinVar RCV Id: RCV000043516
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269580.1:p.Met1Ile
CA143744
NM_001282651.2:c.3G>A
CA412899007
NM_001282651.2:c.3G>T
CA412899009
NM_001282651.2:c.3G>C