Canonical Allele Identifier: PA2826443409
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 228270
ClinVar RCV Id: RCV000223064

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Asp258Glu
CA10576367
NM_001257374.3:c.774C>G
CA342820469
NM_001257374.3:c.774C>A