Canonical Allele Identifier: PA2826657935
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 242002
ClinVar RCV Id: RCV000227837 RCV000597022 RCV001184022 RCV002479935 RCV003998891 RCV004020899
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg338Cys
CA049655
NM_001282624.2:c.1012C>T