Canonical Allele Identifier: PA2826657863
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 647241
ClinVar RCV Id: RCV000801706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg305Gly
CA342820683
NM_001282624.2:c.913A>G