Canonical Allele Identifier: PA2826660601
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 497324
ClinVar RCV Id: RCV000594075 RCV001867919
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Gln493Pro
CA342822801
NM_001282626.2:c.1478A>C