Canonical Allele Identifier: PA103489
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66790
ClinVar RCV Id: RCV000057251 RCV000805453 RCV001257936 RCV004018987
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Arg388His
CA016807
NM_170707.4:c.1163G>A