Canonical Allele Identifier: PA2826658187
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66862
ClinVar RCV Id: RCV000057347 RCV000208352 RCV000454519 RCV000785171 RCV000812762 RCV001004948 RCV001174410 RCV001174246 RCV001185752 RCV003996506
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg464Cys
CA017642
NM_001282624.2:c.1390C>T