Canonical Allele Identifier: PA2826660555
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1338284
ClinVar RCV Id: RCV001817655

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Asn466Asp
CA342822454
NM_001282626.2:c.1396A>G