Canonical Allele Identifier: PA2827264778
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 372787
ClinVar RCV Id: RCV000413411
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316075.1:p.Arg171Gly
CA16042468
NM_001329146.2:c.511A>G