Canonical Allele Identifier: PA108548
Gene: SNTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 8476
ClinVar RCV Id: RCV000008997 RCV000414434 RCV000852541 RCV002326671 RCV002512925
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003089.1:p.Ala390Val
CA254410
NM_003098.3:c.1169C>T