Allele Registry

Canonical Allele Identifier: PA104202

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000015627

RCV000057357

ClinVar Variation:

18457

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Leu59Arg	CA017717 NM_170707.4:c.176T>G