Canonical Allele Identifier: PA302254
Gene: SNTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 190907
ClinVar RCV Id: RCV000656979 RCV000540961 RCV000781872 RCV002492708 RCV002433740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003089.1:p.Gly96Ala
CA302252
NM_003098.3:c.287G>C