Canonical Allele Identifier: PA2826657672
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66952
ClinVar RCV Id: RCV000057481 RCV000146262 RCV001234965 RCV003227631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Asp219Asn
CA018826
NM_001282624.2:c.655G>A