Allele Registry

Canonical Allele Identifier: PA2826657719

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV001324030

ClinVar Variation:

1023912

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Ser245Ala	CA342820087 NM_001282624.2:c.733T>G