Canonical Allele Identifier: PA2826660393
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 435771
ClinVar RCV Id: RCV000501231
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg388Pro
CA342820778
NM_001282626.2:c.1163G>C