ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2827264705
Gene: TP63
HGNC
NCBI
Linked Data
ClinVar Variation Id:
478110
ClinVar RCV Id:
RCV000559680
RCV000851194
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001316075.1:p.His68Tyr
CA355753773
NM_001329146.2:c.202C>T