Canonical Allele Identifier: PA2827402159
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1256377

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334630.1:p.Ser602Ile
CA4052901
NM_001347701.2:c.1805G>T