Canonical Allele Identifier: PA111128
Gene: SOX17 HGNC NCBI

Linked Data

ClinVar Variation Id: 18413
ClinVar RCV Id: RCV000001140 RCV000430409 RCV000895009 RCV003924848
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071899.1:p.Tyr259Asn
CA114741
NM_022454.4:c.775T>A