Allele Registry

Canonical Allele Identifier: PA1139757419

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV001238528

ClinVar Variation:

964333

HGVS (amino-acid)	Matching Registered Transcripts
NP_733822.1:p.Arg482Gly	CA342822665 NM_170708.4:c.1444C>G