Canonical Allele Identifier: PA2826657497
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2413543
ClinVar RCV Id: RCV003104339

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg144Pro
CA342817173
NM_001282624.2:c.431G>C