Canonical Allele Identifier: PA207692
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66828
ClinVar RCV Id: RCV000057301
ClinVar Variation Id: 66829
ClinVar RCV Id: RCV000057302 RCV000193901
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Lys486Asn
CA017278
NM_005572.4:c.1458G>C
CA017283
NM_005572.4:c.1458G>T