Canonical Allele Identifier: PA2826443485
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 408997

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Arg276_Pro281dup
CA16609880
NM_001257374.3:c.825_842dup