Canonical Allele Identifier: PA2826659908
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 163866

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg166Gln
CA018161
NM_001282626.2:c.497G>A