Canonical Allele Identifier: PA2826657394
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2765842
ClinVar RCV Id: RCV003583110

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Asp83Asn
CA342815629
NM_001282624.2:c.247G>A