Canonical Allele Identifier: PA2826658229
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 200928
ClinVar RCV Id: RCV000182349 RCV000664076 RCV000778037 RCV001701632 RCV004020193 RCV000852591 RCV001852310 RCV002464010
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg490His
CA017707
NM_001282624.2:c.1469G>A