Canonical Allele Identifier: PA2826922722
Gene: SNCAIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2277017
ClinVar RCV Id: RCV004124826
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295034.1:p.Leu666Met
CA3385046
NM_001308105.1:c.1996T>A