Canonical Allele Identifier: PA270630
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 144046
ClinVar RCV Id: RCV000133551 RCV000513734
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138737.1:p.Phe155del
CA270628
NM_001145265.2:c.464_466del