Allele Registry

Canonical Allele Identifier: PA2826660808

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000041334

RCV000057361

RCV000148601

RCV000617798

RCV000771799

RCV001088263

RCV004541208

ClinVar Variation:

48052

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Gly602Ser	CA014839 NM_001282626.2:c.1804G>A