Canonical Allele Identifier: PA217847
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Pro4Arg
CA016863
NM_005572.4:c.11C>G