Canonical Allele Identifier: PA2826659089
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 498978

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Glu372Lys
CA342820494
NM_001282625.2:c.1114G>A