Canonical Allele Identifier: PA209919
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 198681

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_892006.3:p.Val5113Ile
CA209917
NM_182961.4:c.15337G>A