Canonical Allele Identifier: PA261942
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 48028
ClinVar RCV Id: RCV000041305 RCV000236658 RCV002513581
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Leu369Pro
CA016599
NM_170707.4:c.1106T>C