Canonical Allele Identifier: PA261978
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 48046
ClinVar RCV Id: RCV000057343 RCV000041325 RCV000211786 RCV000242991 RCV000462793
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Arg541Cys
CA017615
NM_170707.4:c.1621C>T