Canonical Allele Identifier: PA103767
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66811
ClinVar RCV Id: RCV000057277 RCV000465598
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Asn456Asp
CA017074
NM_170707.4:c.1366A>G