Canonical Allele Identifier: PA658812805
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 521983

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Arg582Leu
CA342826551
NM_170707.4:c.1745G>T