Allele Registry

Canonical Allele Identifier: PA2826660293

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV002295209

ClinVar Variation:

1722182

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Ala350Val	CA342820270 NM_001282626.2:c.1049C>T