Canonical Allele Identifier: PA2742006600
Gene: SYN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2662200
ClinVar RCV Id: RCV003443695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_598006.1:p.Ser605Arg
CA412822485
NM_133499.2:c.1815C>G
CA412822486
NM_133499.2:c.1815C>A
CA412822493
NM_133499.2:c.1813A>C