Canonical Allele Identifier: PA2580111967
Gene: SOX9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2222804

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000337.1:p.Pro354_Pro356dup
CA2273926519
NM_000346.4:c.1061_1069dup