Canonical Allele Identifier: PA2826660796
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_001269555.1:p.Asp596Asn
CA051326
NM_001282626.2:c.1786G>A