Canonical Allele Identifier: PA658807966
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 538375
ClinVar RCV Id: RCV000647610

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Asp5619Gly
CA7223514
NM_182914.2:c.16856A>G