Canonical Allele Identifier: PA123455
Gene: PAX9 HGNC NCBI

Linked Data

ClinVar Variation Id: 13781
ClinVar RCV Id: RCV000014791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006185.1:p.Arg47Trp
CA123454
NM_006194.4:c.139C>T