Canonical Allele Identifier: PA2830329998
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 435774
ClinVar RCV Id: RCV000503392 RCV000653834 RCV000992277 RCV001526033 RCV004003526
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Asp566Asn
CA051326
NM_170708.4:c.1696G>A