Canonical Allele Identifier: PA302284
Gene: SNTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 190918
ClinVar RCV Id: RCV000171101 RCV000243691 RCV000656217 RCV000796538 RCV001138961 RCV003155101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003089.1:p.Glu363Ala
CA302282
NM_003098.3:c.1088A>C