Canonical Allele Identifier: PA2826657967
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66802
ClinVar RCV Id: RCV000057265 RCV000150953 RCV000148606 RCV000653929 RCV001172619 RCV001524022 RCV002381364
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg354Cys
CA014967
NM_001282624.2:c.1060C>T