Canonical Allele Identifier: PA2580111945
Gene: SOX9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2024289
ClinVar RCV Id: RCV002863207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000337.1:p.Pro266Leu
CA400867062
NM_000346.4:c.797C>T