Canonical Allele Identifier: PA2827281493
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 1413071
ClinVar RCV Id: RCV001925684
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316893.1:p.Thr189Ser
CA355750847
NM_001329964.2:c.565A>T
CA355750849
NM_001329964.2:c.566C>G