Canonical Allele Identifier: PA2826658765
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1978461
ClinVar RCV Id: RCV002775064

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Val227Met
CA342817182
NM_001282625.2:c.679G>A