Canonical Allele Identifier: PA645421168
Gene: SNTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 430498
ClinVar RCV Id: RCV000493858
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003089.1:p.Gly18Arg
CA408634707
NM_003098.3:c.52G>C
CA408634708
NM_003098.3:c.52G>A