Canonical Allele Identifier: PA2826658522
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 424916
ClinVar RCV Id: RCV000487579 RCV001184326 RCV002525984 RCV004003411
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Arg110Ser
CA16621577
NM_001282625.2:c.328C>A