Allele Registry

Canonical Allele Identifier: PA123455

Gene: PAX9 HGNC NCBI

ClinVar RCV:

RCV000014791

ClinVar Variation:

13781

HGVS (amino-acid)	Matching Registered Transcripts
NP_006185.1:p.Arg47Trp	CA123454 NM_006194.4:c.139C>T