Allele Registry

Canonical Allele Identifier: PA2826658755

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000015583

RCV000057440

RCV002286398

ClinVar Variation:

14492

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269554.1:p.His222Tyr	CA018412 NM_001282625.2:c.664C>T