Canonical Allele Identifier: PA2828468263
Gene: PAX9 HGNC NCBI

Linked Data

ClinVar Variation Id: 155939
ClinVar RCV Id: RCV000144943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001359005.1:p.Cys112Trp
CA171021
NM_001372076.1:c.336C>G