Canonical Allele Identifier: PA645486558
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 282872

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Thr4617Ile
CA7222586
NM_182914.2:c.13850C>T