Canonical Allele Identifier: PA2826660316
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1462026
ClinVar RCV Id: RCV001968252
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Asp357Glu
CA342820316
NM_001282626.2:c.1071C>A
CA342820317
NM_001282626.2:c.1071C>G