Canonical Allele Identifier: PA2827265340
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 1451179
ClinVar RCV Id: RCV002007150
ClinVar Variation Id: 1475057
ClinVar RCV Id: RCV001973838
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316077.1:p.Phe561Leu
CA355759032
NM_001329148.2:c.1681T>C
CA355759040
NM_001329148.2:c.1683C>A
CA355759043
NM_001329148.2:c.1683C>G