Canonical Allele Identifier: PA2828468252
Gene: PAX9 HGNC NCBI

Linked Data

ClinVar Variation Id: 13770

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001359005.1:p.Lys91Glu
CA123443
NM_001372076.1:c.271A>G