Canonical Allele Identifier: PA217859
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66797

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Val415Ile
CA016913
NM_170707.4:c.1243G>A