Canonical Allele Identifier: PA2830422337
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 282661

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878917.1:p.Ala369Thr
CA7224740
NM_182913.2:c.1105G>A