Canonical Allele Identifier: PA2826657721
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 48097
ClinVar RCV Id: RCV000057494 RCV000212504 RCV000208012 RCV000544253 RCV000621488 RCV000755678 RCV001192112 RCV003996467
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Ser245Thr
CA018917
NM_001282624.2:c.733T>A