Canonical Allele Identifier: PA2829900601
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2013391
ClinVar RCV Id: RCV002856466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060859.4:p.Met14Ile
CA380202016
NM_018389.5:c.42G>A
CA380202017
NM_018389.5:c.42G>C
CA380202019
NM_018389.5:c.42G>T