Canonical Allele Identifier: PA174088
Gene: SOX9 HGNC NCBI

Linked Data

ClinVar Variation Id: 161465
ClinVar RCV Id: RCV000148999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000337.1:p.Ala21Thr
CA174087
NM_000346.4:c.61G>A