Allele Registry

Canonical Allele Identifier: PA2826658069

Gene: LMNA HGNC NCBI

ClinVar Allele:

77725

77726

ClinVar RCV:

RCV000057301

RCV000057302

RCV000193901

ClinVar Variation:

66828

66829

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Lys405Asn	CA017278 NM_001282624.2:c.1215G>C CA017283 NM_001282624.2:c.1215G>T