Canonical Allele Identifier: PA2825339081
Gene: SC5D HGNC NCBI

Linked Data

ClinVar Variation Id: 1967586
ClinVar RCV Id: RCV002754960
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020127.1:p.Ile182Met
CA6328194
NM_001024956.3:c.546A>G