Canonical Allele Identifier: PA2826658559
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2587216
ClinVar RCV Id: RCV003360741

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Lys123Asn
CA342815028
NM_001282625.2:c.369G>T
CA342815032
NM_001282625.2:c.369G>C