Canonical Allele Identifier: PA2826442714
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Arg21Leu
CA018044
NM_001257374.3:c.62G>T