Canonical Allele Identifier: PA645486538
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 313574

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Gly4191Asp
CA7222193
NM_182914.2:c.12572G>A