Canonical Allele Identifier: PA302239
Gene: SNTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 190902
ClinVar RCV Id: RCV002307430
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003089.1:p.Pro8Ala
CA302237
NM_003098.3:c.22C>G