Canonical Allele Identifier: PA2825580287
Gene: TP63 HGNC NCBI
ClinVar RCV:
RCV000190455
ClinVar Variation:
208418
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108452.1:p.Ala252Gly
CA204448
NM_001114980.1:c.755C>G