Canonical Allele Identifier: PA2826659755
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 292835
ClinVar RCV Id: RCV000274541 RCV000281871 RCV000294652 RCV000301985 RCV000329877 RCV000335629 RCV000337024 RCV000342879 RCV000371803 RCV000389042 RCV000497577 RCV001096351 RCV003231436
ClinVar Variation Id: 2428009
ClinVar RCV Id: RCV003116980
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg99Ser
CA10607825
NM_001282626.2:c.295C>A
CA2580061181
NM_001282626.2:c.294_295delinsAA