Canonical Allele Identifier: PA915972046
Gene: CDSN HGNC NCBI

Linked Data

ClinVar Variation Id: 716865
ClinVar RCV Id: RCV000889576 RCV003930753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255.4:p.Asn179Ser
CA3708477
NM_001264.5:c.536A>G