Canonical Allele Identifier: PA2826658768
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14518

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Asp230Asn
CA018460
NM_001282625.2:c.688G>A