Allele Registry

Canonical Allele Identifier: PA2829810765

Gene: SYNE2 HGNC NCBI

ClinVar Variation Id: 313670

HGVS (amino-acid)	Matching Registered Transcripts
NP_055995.4:p.Thr6879Asn	CA7224998 NM_015180.5:c.20636C>A