Canonical Allele Identifier: PA2826659714
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 543218
ClinVar RCV Id: RCV000653914 RCV001289082
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Tyr81His
CA342808404
NM_001282626.2:c.241T>C