Canonical Allele Identifier: PA2826657979
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 519022

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Val361Met
CA049885
NM_001282624.2:c.1081G>A