Canonical Allele Identifier: PA2826443218
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66952

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Asp188Asn
CA018826
NM_001257374.3:c.562G>A