Canonical Allele Identifier: PA915979718
Gene: SNTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 811698
ClinVar RCV Id: RCV001001979 RCV003372937
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003089.1:p.Gln153His
CA408633367
NM_003098.3:c.459G>T
CA408633368
NM_003098.3:c.459G>C