Canonical Allele Identifier: PA108536
Gene: SNTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 191548
ClinVar RCV Id: RCV000171774 RCV000191018 RCV000247418 RCV000990299 RCV001706109 RCV001256962 RCV003917588
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003089.1:p.Ala257Gly
CA199841
NM_003098.3:c.770C>G