Canonical Allele Identifier: PA2829412327
Gene: SNTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3167061
ClinVar RCV Id: RCV004464426
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003089.1:p.Ala23Ser
CA408634657
NM_003098.3:c.67G>T