Canonical Allele Identifier: PA2826660707
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66862
ClinVar RCV Id: RCV000057347 RCV000208352 RCV000454519 RCV000785171 RCV000812762 RCV001004948 RCV001174410 RCV001174246 RCV001185752 RCV003996506
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg545Cys
CA017642
NM_001282626.2:c.1633C>T