Canonical Allele Identifier: PA2826659130
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66789

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Arg388Cys
CA016798
NM_001282625.2:c.1162C>T