Canonical Allele Identifier: PA346673
Gene: SNTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 180529
ClinVar RCV Id: RCV000157506 RCV001058598 RCV002408707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003089.1:p.Arg274Gln
CA346671
NM_003098.3:c.821G>A