ClinGen Allele Registry
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Canonical Allele Identifier:
PA2828468190
Gene: PAX9
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000014781
ClinVar Variation:
13771
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001359005.1:p.Leu21Pro
CA123445
NM_001372076.1:c.62T>C