Allele Registry

Canonical Allele Identifier: PA658813215

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000593108

RCV001387373

ClinVar Variation:

502242

HGVS (amino-acid)	Matching Registered Transcripts
NP_733822.1:p.Asp446Gly	CA342822060 NM_170708.4:c.1337A>G