Canonical Allele Identifier: PA111889
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6545
ClinVar RCV Id: RCV000006920
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003713.3:p.Ser580Pro
CA118343
NM_003722.5:c.1738T>C