Canonical Allele Identifier: PA1139724382
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 860772
ClinVar RCV Id: RCV001067142

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060859.4:p.Asp64Glu
CA380202470
NM_018389.5:c.192C>A
CA380202471
NM_018389.5:c.192C>G