Canonical Allele Identifier: PA2499296769
Gene: SYN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1187026
ClinVar RCV Id: RCV001546338
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_598006.1:p.Ala542Thr
CA412823084
NM_133499.2:c.1624G>A