Allele Registry

Canonical Allele Identifier: PA2825609920

Gene: TP53 HGNC NCBI

ClinVar Allele:

420659

ClinVar RCV:

RCV000492442

RCV000702915

RCV004023278

ClinVar Variation:

428866

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119587.1:p.His36Arg	CA287488569 NM_001126115.1:c.107A>G