Allele Registry

Canonical Allele Identifier: PA2826660695

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000057340

RCV000192012

ClinVar Variation:

66858

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Met540Thr	CA017588 NM_001282626.2:c.1619T>C