Canonical Allele Identifier: PA2826658894
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 598133
ClinVar RCV Id: RCV000734453 RCV000793720
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.His289Pro
CA342817658
NM_001282625.2:c.866A>C