Allele Registry

Canonical Allele Identifier: PA2826657773

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV002295209

ClinVar Variation:

1722182

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Ala269Val	CA342820270 NM_001282624.2:c.806C>T