Canonical Allele Identifier: PA2826660339
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 228270
ClinVar RCV Id: RCV000223064

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Asp370Glu
CA10576367
NM_001282626.2:c.1110C>G
CA342820469
NM_001282626.2:c.1110C>A