Canonical Allele Identifier: PA916029168
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 593818

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334631.1:p.Thr969Lys
CA4052578
NM_001347702.2:c.2906C>A