Canonical Allele Identifier: PA645486591
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 282892

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Asp5283Gly
CA7223206
NM_182914.2:c.15848A>G