Allele Registry

Canonical Allele Identifier: PA2825802535

Gene: SYN3 HGNC NCBI

ClinVar Allele:

362165

ClinVar RCV:

RCV000416436

ClinVar Variation:

375384

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129246.1:p.Pro481Leu	CA16044239 NM_001135774.2:c.1441_1442delinsTT CA411339019 NM_001135774.2:c.1442C>T