Canonical Allele Identifier: PA231536
Gene: SYN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 130384
ClinVar RCV Id: RCV000118424
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008881.2:p.Gly541Arg
CA231535
NM_006950.3:c.1621G>C
CA412823092
NM_006950.3:c.1621G>A