Canonical Allele Identifier: PA645438225
Gene: SOX9 HGNC NCBI
ClinVar RCV:
RCV000415154
ClinVar Variation:
374384
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000337.1:p.Met476Thr
CA16043696
NM_000346.4:c.1427T>C