Canonical Allele Identifier: PA2580336636
Gene: PAX9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1721820
ClinVar RCV Id: RCV002302192

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006185.1:p.Val83Gly
CA389466427
NM_006194.4:c.248T>G