Canonical Allele Identifier: PA302323
Gene: SNTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 190932
ClinVar RCV Id: RCV000171115 RCV000246049 RCV000458749 RCV001804901 RCV002485082
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003089.1:p.Glu14Lys
CA302321
NM_003098.3:c.40G>A