Canonical Allele Identifier: PA2828468231
Gene: PAX9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1693562
ClinVar RCV Id: RCV002260957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001359005.1:p.Gly64Val
CA389466309
NM_001372076.1:c.191G>T