Canonical Allele Identifier: PA2826658750
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 950917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Arg221His
CA054078
NM_001282625.2:c.662G>A