Canonical Allele Identifier: PA262024
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 48097
ClinVar RCV Id: RCV000057494 RCV000212504 RCV000208012 RCV000544253 RCV000621488 RCV000755678 RCV001192112 RCV003996467
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Ser326Thr
CA018917
NM_170707.4:c.976T>A