Canonical Allele Identifier: PA124029
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14493
ClinVar RCV Id: RCV000015584 RCV000057287 RCV001851878
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Gly465Asp
CA017164
NM_170708.4:c.1394G>A