Canonical Allele Identifier: PA2826658079
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 497324

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Gln412Pro
CA342822801
NM_001282624.2:c.1235A>C