Canonical Allele Identifier: PA235721
Gene: SNTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 190914
ClinVar RCV Id: RCV000171097 RCV000185526 RCV000206185 RCV000266318 RCV000678949 RCV002408740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003089.1:p.Ala263Ser
CA235719
NM_003098.3:c.787G>T