Canonical Allele Identifier: PA2826660764
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 521983

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg582Leu
CA342826551
NM_001282626.2:c.1745G>T