Canonical Allele Identifier: PA2829681610
Gene: SYN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2902261
ClinVar RCV Id: RCV003622075

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008881.2:p.Gln635His
CA412822209
NM_006950.3:c.1905G>T
CA412822211
NM_006950.3:c.1905G>C