Canonical Allele Identifier: PA123452
Gene: PAX9 HGNC NCBI

Linked Data

ClinVar Variation Id: 13775

Amino-acid Alleles

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