Canonical Allele Identifier: PA2825884431
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2807192
ClinVar RCV Id: RCV003612586

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138737.1:p.Ser7Pro
CA380202079
NM_001145265.2:c.19T>C