Canonical Allele Identifier: PA2829810021
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 289931

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055995.4:p.Lys5632Glu
CA7223523
NM_015180.5:c.16894A>G