Canonical Allele Identifier: PA217849
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Pro4Arg
CA016863
NM_170708.4:c.11C>G