Canonical Allele Identifier: PA2826657846
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2974892
ClinVar RCV Id: RCV003838514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Leu299Met
CA342820594
NM_001282624.2:c.895T>A