Allele Registry

Canonical Allele Identifier: PA2826442737

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000015604

RCV000057405

ClinVar Variation:

14510

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Ser31Phe	CA018089 NM_001257374.3:c.92C>T