Canonical Allele Identifier: PA2829469696
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 1684042
ClinVar RCV Id: RCV002244562
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003713.3:p.Lys188_Ala190del
CA2573136832
NM_003722.5:c.563_571del