Canonical Allele Identifier: PA2829810013
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 538375
ClinVar RCV Id: RCV000647610

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055995.4:p.Asp5619Gly
CA7223514
NM_015180.5:c.16856A>G