Canonical Allele Identifier: PA2829681566
Gene: SYN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2919071
ClinVar RCV Id: RCV003622383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008881.2:p.Pro572Gln
CA412822805
NM_006950.3:c.1715C>A