Canonical Allele Identifier: PA2826658045
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 36476

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg390His
CA017220
NM_001282624.2:c.1169G>A