Allele Registry

Canonical Allele Identifier: PA2829603467

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV001324030

ClinVar Variation:

1023912

HGVS (amino-acid)	Matching Registered Transcripts
NP_005563.1:p.Ser326Ala	CA342820087 NM_005572.4:c.976T>G