Allele Registry

Canonical Allele Identifier: PA645486636

Gene: SYNE2 HGNC NCBI

ClinVar RCV:

RCV000271387

RCV000518669

ClinVar Variation:

313647

HGVS (amino-acid)	Matching Registered Transcripts
NP_878918.2:p.Arg6379His	CA7224329 NM_182914.2:c.19136G>A