Allele Registry

Canonical Allele Identifier: PA2826443900

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000057340

RCV000192012

ClinVar Variation:

66858

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Met428Thr	CA017588 NM_001257374.3:c.1283T>C