Canonical Allele Identifier: PA645438205
Gene: SOX9 HGNC NCBI

Linked Data

ClinVar Variation Id: 373438
ClinVar RCV Id: RCV000413454
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000337.1:p.Arg160Pro
CA16043055
NM_000346.4:c.479G>C