Allele Registry

Canonical Allele Identifier: PA1139755967

Gene: LMNA HGNC NCBI

ClinVar Variation Id: 921978

HGVS (amino-acid)	Matching Registered Transcripts
NP_733822.1:p.Thr3Asn	CA342805896 NM_170708.4:c.8C>A