Canonical Allele Identifier: PA2826660291
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66763
ClinVar RCV Id: RCV000057219 RCV001854172 RCV003343625
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg349Leu
CA016488
NM_001282626.2:c.1046G>T