Canonical Allele Identifier: PA124089
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14520
ClinVar RCV Id: RCV000015617 RCV000057268 RCV001186220 RCV001172618 RCV001264435 RCV000552191 RCV003996102 RCV002381252
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Val440Met
CA016999
NM_170707.4:c.1318G>A