Canonical Allele Identifier: PA2826657421
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66908
ClinVar RCV Id: RCV000057419 RCV000491585 RCV000535082 RCV000619878 RCV003996512 RCV004528262
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg109Trp
CA018245
NM_001282624.2:c.325C>T