Canonical Allele Identifier: PA217899
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66805
ClinVar RCV Id: RCV000057269 RCV001248144
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Asp446Val
CA017008
NM_170708.4:c.1337A>T