Canonical Allele Identifier: PA916013552
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66899
ClinVar RCV Id: RCV000057404 RCV001387327 RCV001258042 RCV003996511
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Ser62Pro
CA018081
NM_001282624.2:c.184T>C