Canonical Allele Identifier: PA2826658642
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2765842
ClinVar RCV Id: RCV003583110
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Asp164Asn
CA342815629
NM_001282625.2:c.490G>A