Allele Registry

Canonical Allele Identifier: PA2829810648

Gene: SYNE2 HGNC NCBI

ClinVar RCV:

RCV000647578

RCV004025742

ClinVar Variation:

538357

HGVS (amino-acid)	Matching Registered Transcripts
NP_055995.4:p.Gln6724Pro	CA7224796 NM_015180.5:c.20171A>C