Allele Registry

Canonical Allele Identifier: PA2826563347

Gene: TP53 HGNC NCBI

ClinVar Variation Id: 216469

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263627.1:p.Tyr77His	CA338059 NM_001276698.3:c.229T>C