Allele Registry

Canonical Allele Identifier: PA2828371642

Gene: SYN3 HGNC NCBI

ClinVar RCV:

RCV000416436

ClinVar Variation:

375384

HGVS (amino-acid)	Matching Registered Transcripts
NP_001356838.1:p.Pro481Leu	CA16044239 NM_001369909.1:c.1441_1442delinsTT CA411339019 NM_001369909.1:c.1442C>T