Canonical Allele Identifier: PA2827265713
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 2635464
ClinVar RCV Id: RCV003418980
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316079.1:p.Cys166Phe
CA355755174
NM_001329150.2:c.497G>T