Canonical Allele Identifier: PA2826658277
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 523026
ClinVar RCV Id: RCV000626229 RCV003581701
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Pro20Leu
CA342807133
NM_001282625.2:c.59C>T