Canonical Allele Identifier: PA2825362166
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2836762
ClinVar RCV Id: RCV003741998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027460.1:p.Thr174Ser
CA412894084
NM_001032289.3:c.521C>G
CA412894086
NM_001032289.3:c.520A>T