Canonical Allele Identifier: PA2825884699
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2096091
ClinVar RCV Id: RCV003013995
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138738.1:p.Met114Ile
CA380202854
NM_001145266.1:c.342G>A
CA380202855
NM_001145266.1:c.342G>C
CA380202856
NM_001145266.1:c.342G>T