Allele Registry

Canonical Allele Identifier: PA123450

Gene: PAX9 HGNC NCBI

ClinVar RCV:

RCV000014784

RCV003591632

ClinVar Variation:

13774

HGVS (amino-acid)	Matching Registered Transcripts
NP_006185.1:p.Arg26Trp	CA123449 NM_006194.4:c.76C>T