Canonical Allele Identifier: PA2741851802
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2663778
ClinVar RCV Id: RCV003885329

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269580.1:p.Leu335_Val338dup
CA2740092153
NM_001282651.2:c.1002_1013dup