Canonical Allele Identifier: PA2580402451
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2096091
ClinVar RCV Id: RCV003013995

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060859.4:p.Met127Ile
CA380202854
NM_018389.5:c.381G>A
CA380202855
NM_018389.5:c.381G>C
CA380202856
NM_018389.5:c.381G>T