Canonical Allele Identifier: PA218089
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66858
ClinVar RCV Id: RCV000057340 RCV000192012
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Met540Thr
CA017588
NM_170707.4:c.1619T>C