Allele Registry

Canonical Allele Identifier: PA2828371599

Gene: SYN3 HGNC NCBI

ClinVar RCV:

RCV000416436

ClinVar Variation:

375384

HGVS (amino-acid)	Matching Registered Transcripts
NP_001356837.1:p.Pro482Leu	CA16044239 NM_001369908.1:c.1444_1445delinsTT CA411339019 NM_001369908.1:c.1445C>T