Canonical Allele Identifier: PA204449
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 208418
ClinVar RCV Id: RCV000190455
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003713.3:p.Ala346Gly
CA204448
NM_003722.5:c.1037C>G