Canonical Allele Identifier: PA2741899668
Gene: SNTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2562678
ClinVar RCV Id: RCV003296671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003089.1:p.Leu113Arg
CA408633625
NM_003098.3:c.338T>G