Allele Registry

Canonical Allele Identifier: PA104121

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000057402

RCV001854176

ClinVar Variation:

66898

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Leu140Pro	CA018070 NM_170707.4:c.419T>C