Allele Registry

Canonical Allele Identifier: PA2830327562

Gene: LMNA HGNC NCBI

ClinVar Allele:

442638

ClinVar RCV:

RCV000523012

RCV000695647

RCV002341216

RCV003532151

RCV004003591

ClinVar Variation:

449052

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Arg397His	CA049391 NM_170707.4:c.1190G>A