Canonical Allele Identifier: PA2826658009
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66810

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg374Pro
CA017066
NM_001282624.2:c.1121G>C