Canonical Allele Identifier: PA217987
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66824

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Arg471Gly
CA017206
NM_005572.4:c.1411C>G