Canonical Allele Identifier: PA2830326582
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 574040

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Arg166Trp
CA053599
NM_170707.4:c.496C>T