Canonical Allele Identifier: PA645438218
Gene: SOX9 HGNC NCBI

Linked Data

ClinVar Variation Id: 324918

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000337.1:p.Pro346dup
CA8739077
NM_000346.4:c.1029_1031dup
CA2810344962
NM_000346.4:c.1035_1037dup