Canonical Allele Identifier: PA2826443698
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 488542
ClinVar RCV Id: RCV000578339
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Gln350Pro
CA342822406
NM_001257374.3:c.1049A>C