Canonical Allele Identifier: PA1139735779
Gene: SLC35D1 HGNC NCBI

Linked Data

ClinVar Variation Id: 965733
ClinVar RCV Id: RCV001240249

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055954.1:p.Glu28Asp
CA899181
NM_015139.3:c.84G>C
CA340708646
NM_015139.3:c.84G>T