Canonical Allele Identifier: PA2826659386
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 936743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Asn518Asp
CA31014347
NM_001282625.2:c.1552A>G