Canonical Allele Identifier: PA118737
Gene: SC5D HGNC NCBI

Linked Data

ClinVar Variation Id: 7355
ClinVar RCV Id: RCV000007780
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008849.2:p.Gly211Asp
CA118736
NM_006918.5:c.632G>A