Allele Registry

Canonical Allele Identifier: PA2826660708

Gene: LMNA HGNC NCBI

Linked Data

ClinVar RCV:

RCV000150955

RCV000449630

RCV000468904

RCV000491650

RCV000505801

RCV000621850

RCV000771819

RCV001100810

RCV001101055

RCV001101057

RCV001101058

RCV001101059

RCV001101060

RCV001101061

RCV001101062

RCV001248958

RCV001781492

RCV003993830

RCV003998208

RCV004532675

ClinVar Variation:

163878

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Arg545His	CA017649 NM_001282626.2:c.1634G>A