Canonical Allele Identifier: PA2826658049
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1522462
ClinVar RCV Id: RCV002034441
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Asp394Gly
CA342822584
NM_001282624.2:c.1181A>G