Canonical Allele Identifier: PA2829900600
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1053802
ClinVar RCV Id: RCV001362194

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060859.4:p.Met14Val
CA380202010
NM_018389.5:c.40A>G