Canonical Allele Identifier: PA2826657787
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2756516
ClinVar RCV Id: RCV003582948

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Gln274Lys
CA342820300
NM_001282624.2:c.820C>A