Canonical Allele Identifier: PA2826657818
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 228270
ClinVar RCV Id: RCV000223064

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Asp289Glu
CA10576367
NM_001282624.2:c.867C>G
CA342820469
NM_001282624.2:c.867C>A