Canonical Allele Identifier: PA2825580301
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 2883542
ClinVar RCV Id: RCV003757997

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108452.1:p.Ser271Leu
CA89746785
NM_001114980.1:c.812C>T