Allele Registry

Canonical Allele Identifier: PA2829421847

Gene: SYN2 HGNC NCBI

ClinVar RCV:

RCV004098594

ClinVar Variation:

2237597

HGVS (amino-acid)	Matching Registered Transcripts
NP_003169.2:p.Ile203Thr	CA2257361 NM_003178.6:c.608T>C