Canonical Allele Identifier: PA2826659435
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66858
ClinVar RCV Id: RCV000057340 RCV000192012
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Met540Thr
CA017588
NM_001282625.2:c.1619T>C