Canonical Allele Identifier: PA2826658343
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 408994

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Arg41His
CA16609885
NM_001282625.2:c.122G>A