Canonical Allele Identifier: PA235718
Gene: SNTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 180528
ClinVar RCV Id: RCV000157505 RCV000171082 RCV000225771 RCV000618960 RCV003224177
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003089.1:p.Thr262Pro
CA235716
NM_003098.3:c.784A>C