Canonical Allele Identifier: PA111672
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6527
ClinVar RCV Id: RCV000006900 RCV000394306 RCV000812084 RCV002283440
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003713.3:p.Arg243Trp
CA118334
NM_003722.5:c.727C>T