Canonical Allele Identifier: PA2827264209
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 2199304
ClinVar RCV Id: RCV002634280
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316073.1:p.Ile225Thr
CA2752225
NM_001329144.2:c.674T>C