Canonical Allele Identifier: PA302266
Gene: SNTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 190911
ClinVar RCV Id: RCV000171094 RCV000780741 RCV000558137 RCV002362873 RCV003975245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003089.1:p.Cys226Tyr
CA302264
NM_003098.3:c.677G>A