Canonical Allele Identifier: PA645423401
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_003713.3:p.Cys347Phe
CA16617858
NM_003722.5:c.1040G>T