Canonical Allele Identifier: PA2826660256
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 245682
ClinVar RCV Id: RCV000236116 RCV001176603 RCV001857795 RCV002379039 RCV003227732 RCV003998898
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg331Trp
CA10584124
NM_001282626.2:c.991C>T