Canonical Allele Identifier: PA2830400094
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 355927
ClinVar RCV Id: RCV000292473 RCV000389291 RCV000418802 RCV001069971 RCV004530439
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_892006.3:p.Glu1312Asp
CA4058710
NM_182961.4:c.3936G>C
CA366146705
NM_182961.4:c.3936G>T