Canonical Allele Identifier: PA2830327112
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 502071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Arg298Pro
CA342817795
NM_170707.4:c.893G>C