Canonical Allele Identifier: PA104011
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 48052
ClinVar RCV Id: RCV000041334 RCV000057361 RCV000148601 RCV000771799 RCV000617798 RCV001088263 RCV004541208
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Gly602Ser
CA014839
NM_170707.4:c.1804G>A