Canonical Allele Identifier: PA2826661702
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 509462
ClinVar RCV Id: RCV000651310 RCV000606151 RCV003437306
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269577.1:p.Arg139His
CA10406060
NM_001282648.2:c.416G>A