Canonical Allele Identifier: PA658678050
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 470933

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Arg4636Cys
CA261849912
NM_182914.2:c.13906C>T