Canonical Allele Identifier: PA2826658608
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 48065
ClinVar RCV Id: RCV000041348 RCV000206666
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Ala146Thr
CA018101
NM_001282625.2:c.436G>A