Canonical Allele Identifier: PA915982711
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14484
ClinVar RCV Id: RCV000015573 RCV000057428 RCV000211791 RCV003581565
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Glu91Gly
CA018298
NM_001257374.3:c.272A>G