Canonical Allele Identifier: PA2828468207
Gene: PAX9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1119978
ClinVar RCV Id: RCV001449584

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001359005.1:p.Gly51Val
CA389466223
NM_001372076.1:c.152G>T