Allele Registry

Canonical Allele Identifier: PA2825618692

Gene: TP53 HGNC NCBI

ClinVar Variation Id: 647256

ClinVar RCV Id: RCV000801729

ClinVar Variation Id: 2113149

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119590.1:p.Ser230Arg	CA397837062 NM_001126118.1:c.690C>G CA397837064 NM_001126118.1:c.690C>A CA397837083 NM_001126118.1:c.688A>C