Canonical Allele Identifier: PA2499245337
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1171092
ClinVar RCV Id: RCV001523989

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Ile47Val
CA342815101
NM_001282624.2:c.139A>G