Canonical Allele Identifier: PA2829900608
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2807192
ClinVar RCV Id: RCV003612586
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060859.4:p.Ser20Pro
CA380202079
NM_018389.5:c.58T>C