Allele Registry

Canonical Allele Identifier: PA2825598567

Gene: TP53 HGNC NCBI

ClinVar Variation Id: 642623

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119584.1:p.Gln16His	CA397848970 NM_001126112.3:c.48G>C CA397848971 NM_001126112.3:c.48G>T