Canonical Allele Identifier: PA2827402032
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 76197

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334630.1:p.Asp420Asn
CA4053105
NM_001347701.2:c.1258G>A