Canonical Allele Identifier: PA209942
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 212340

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_892006.3:p.Arg6676Gln
CA209940
NM_182961.4:c.20027G>A