Canonical Allele Identifier: PA2573201412
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 1413071
ClinVar RCV Id: RCV001925684

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316078.1:p.Thr97Ser
CA355750847
NM_001329149.2:c.289A>T
CA355750849
NM_001329149.2:c.290C>G