Canonical Allele Identifier: PA218119
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66865
ClinVar RCV Id: RCV000057356
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Cys558Arg
CA020344
NM_170708.4:c.1672T>C