Allele Registry

Canonical Allele Identifier: PA2826443771

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000594075

RCV001867919

ClinVar Variation:

497324

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Gln381Pro	CA342822801 NM_001257374.3:c.1142A>C