Canonical Allele Identifier: PA2825339076
Gene: SC5D HGNC NCBI

Linked Data

ClinVar Variation Id: 1896514
ClinVar RCV Id: RCV002575794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020127.1:p.His151Arg
CA6328182
NM_001024956.3:c.452A>G