Canonical Allele Identifier: PA916027711
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6537
ClinVar RCV Id: RCV000006911
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316079.1:p.Asn6His
CA340597
NM_001329150.2:c.16A>C