Canonical Allele Identifier: PA2826443628
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Val328Met
CA016999
NM_001257374.3:c.982G>A