Allele Registry

Canonical Allele Identifier: PA2829603477

Gene: LMNA HGNC NCBI

ClinVar Allele:

1002177

ClinVar RCV:

RCV001317047

ClinVar Variation:

1017837

HGVS (amino-acid)	Matching Registered Transcripts
NP_005563.1:p.Glu330Lys	CA342820135 NM_005572.4:c.988G>A