Allele Registry

Canonical Allele Identifier: PA2826659612

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000415420

RCV001861451

ClinVar Variation:

374201

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Val44Phe	CA16043361 NM_001282626.2:c.130G>T