Canonical Allele Identifier: PA2826660508
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_001269555.1:p.Asp446Val
CA017008
NM_001282626.2:c.1337A>T