Allele Registry

Canonical Allele Identifier: PA2826660697

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000022641

RCV000057342

ClinVar Variation:

29775

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Arg541Gly	CA017607 NM_001282626.2:c.1621C>G