Canonical Allele Identifier: PA916013644
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 282611
ClinVar RCV Id: RCV000377201 RCV002429215 RCV002521886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269580.1:p.Leu304Phe
CA10406092
NM_001282651.2:c.910C>T