Canonical Allele Identifier: PA916027717
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 444621
ClinVar RCV Id: RCV000512665
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316079.1:p.Lys54Thr
CA355753628
NM_001329150.2:c.161A>C