Canonical Allele Identifier: PA2825339080
Gene: SC5D HGNC NCBI

Linked Data

ClinVar Variation Id: 733321
ClinVar RCV Id: RCV000908590 RCV001104114
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020127.1:p.Ile182Val
CA6328193
NM_001024956.3:c.544A>G