Canonical Allele Identifier: PA111784
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6541
ClinVar RCV Id: RCV000006915 RCV000326964
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003713.3:p.Asp351Gly
CA118341
NM_003722.5:c.1052A>G