Canonical Allele Identifier: PA913196411
Gene: SOX9 HGNC NCBI

Linked Data

ClinVar Variation Id: 618379
ClinVar RCV Id: RCV001811465 RCV002279516 RCV002067190 RCV003928257
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000337.1:p.Pro345Ser
CA8739079
NM_000346.4:c.1033C>T