Canonical Allele Identifier: PA2830119077
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2436675
ClinVar RCV Id: RCV003139011

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149062.1:p.Asp4632Phe
CA2580075295
NM_033071.3:c.13894_13895delinsTT