Canonical Allele Identifier: PA2826660172
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66950
ClinVar RCV Id: RCV000057478 RCV002444515 RCV002513741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Ser295Pro
CA018804
NM_001282626.2:c.883T>C