Canonical Allele Identifier: PA2826657553
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 48077

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg168Gly
CA018552
NM_001282624.2:c.502C>G