Allele Registry

Canonical Allele Identifier: PA2826659443

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000015603

RCV000057346

ClinVar Variation:

14509

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269554.1:p.Lys542Asn	CA017637 NM_001282625.2:c.1626G>C CA342825399 NM_001282625.2:c.1626G>T