Canonical Allele Identifier: PA2827264774
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 418520
ClinVar RCV Id: RCV000481657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316075.1:p.Cys168Phe
CA16617858
NM_001329146.2:c.503G>T