Allele Registry

Canonical Allele Identifier: PA645486696

Gene: SYNE2 HGNC NCBI

ClinVar Allele:

320890

ClinVar RCV:

RCV000647565

RCV004021601

ClinVar Variation:

313668

HGVS (amino-acid)	Matching Registered Transcripts
NP_878918.2:p.Pro6846Ser	CA7224941 NM_182914.2:c.20536C>T