Canonical Allele Identifier: PA2825580906
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 653417
ClinVar RCV Id: RCV000809190
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108454.1:p.Asn152Lys
CA355753768
NM_001114982.2:c.456C>G
CA355753770
NM_001114982.2:c.456C>A