Canonical Allele Identifier: PA2826657865
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66787
ClinVar RCV Id: RCV000057248
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Leu306Val
CA016782
NM_001282624.2:c.916C>G