Allele Registry

Canonical Allele Identifier: PA2830327201

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV001324030

ClinVar Variation:

1023912

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Ser326Ala	CA342820087 NM_170707.4:c.976T>G