Canonical Allele Identifier: PA2826659623
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 922176
ClinVar RCV Id: RCV001182106
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Asp47Glu
CA342807911
NM_001282626.2:c.141C>A
CA342807915
NM_001282626.2:c.141C>G