Canonical Allele Identifier: PA2826659129
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 245759

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Leu387Pro
CA10584130
NM_001282625.2:c.1160T>C