Canonical Allele Identifier: PA2826443519
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14519

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Arg287Cys
CA016847
NM_001257374.3:c.859C>T