Canonical Allele Identifier: PA2827264749
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6533

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316075.1:p.Arg139His
CA118339
NM_001329146.2:c.416G>A