Canonical Allele Identifier: PA2825144622
Gene: SOX9 HGNC NCBI

Linked Data

ClinVar Variation Id: 3167828
ClinVar RCV Id: RCV004457672
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000337.1:p.Pro367Arg
CA400867710
NM_000346.4:c.1100C>G