Canonical Allele Identifier: PA2580172111
Gene: CDSN HGNC NCBI

Linked Data

ClinVar Variation Id: 2300993
ClinVar RCV Id: RCV002850467
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255.4:p.Arg184Cys
CA3708474
NM_001264.5:c.550C>T