Canonical Allele Identifier: PA2826658178
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66860
ClinVar RCV Id: RCV000057344 RCV000221013 RCV000230467 RCV000246865 RCV001262710 RCV001836636 RCV004018989 RCV003335086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg460His
CA017621
NM_001282624.2:c.1379G>A