Canonical Allele Identifier: PA2826658954
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1202871
ClinVar RCV Id: RCV001568706 RCV001866011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Leu313Pro
CA342819726
NM_001282625.2:c.938T>C