Canonical Allele Identifier: PA199982
Gene: SNTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 191576
ClinVar RCV Id: RCV000171823 RCV000228099 RCV000250468 RCV000756673 RCV000852949 RCV001094617
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003089.1:p.Arg106Gln
CA199980
NM_003098.3:c.317G>A