Canonical Allele Identifier: PA2826659447
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 163878
ClinVar RCV Id: RCV000150955 RCV000468904 RCV000491650 RCV000621850 RCV000449630 RCV000505801 RCV001101061 RCV001100810 RCV001101055 RCV001101062 RCV000771819 RCV001248958 RCV001781492 RCV001101057 RCV001101058 RCV001101059 RCV001101060 RCV003993830 RCV003998208 RCV004532675
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Arg545His
CA017649
NM_001282625.2:c.1634G>A