Canonical Allele Identifier: PA2826442820
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66901

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Arg54Pro
CA018166
NM_001257374.3:c.161G>C