Canonical Allele Identifier: PA2826659521
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66888
ClinVar RCV Id: RCV000015599 RCV000057387 RCV000622546 RCV000502816 RCV000755005
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Thr10Ile
CA017867
NM_001282626.2:c.29C>T