Canonical Allele Identifier: PA916013586
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 574040
ClinVar RCV Id: RCV000695871 RCV002334317 RCV002499247 RCV003999646 RCV003532242
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg85Trp
CA053599
NM_001282624.2:c.253C>T