Allele Registry

Canonical Allele Identifier: PA123452

Gene: PAX9 HGNC NCBI

ClinVar RCV:

RCV000014785

RCV000704798

ClinVar Variation:

13775

HGVS (amino-acid)	Matching Registered Transcripts
NP_006185.1:p.Ile87Phe	CA123451 NM_006194.4:c.259A>T