Allele Registry

Canonical Allele Identifier: PA218507

Gene: LMNA HGNC NCBI

ClinVar Allele:

77843

ClinVar RCV:

RCV000057473

RCV000653924

ClinVar Variation:

66946

HGVS (amino-acid)	Matching Registered Transcripts
NP_733822.1:p.Arg28Trp	CA018743 NM_170708.4:c.82C>T