Canonical Allele Identifier: PA2573088006
Gene: PAX9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1300262
ClinVar RCV Id: RCV001732238
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006185.1:p.Gly73Val
CA389466364
NM_006194.4:c.218G>T