Allele Registry

Canonical Allele Identifier: PA2826560783

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV001302774

ClinVar Variation:

1005829

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263625.1:p.Leu98Val	CA397842729 NM_001276696.3:c.292C>G