Canonical Allele Identifier: PA124088
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14520
ClinVar RCV Id: RCV000015617 RCV000057268 RCV001186220 RCV001172618 RCV001264435 RCV000552191 RCV003996102 RCV002381252
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Val440Met
CA016999
NM_005572.4:c.1318G>A