Canonical Allele Identifier: PA339767
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 208163
ClinVar RCV Id: RCV000206266 RCV000312203 RCV000821003
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108450.1:p.His247Arg
CA339766
NM_001114978.2:c.740A>G