Allele Registry

Canonical Allele Identifier: PA2825617689

Gene: TP53 HGNC NCBI

ClinVar Variation Id: 919322

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119590.1:p.Met130Ile	CA397841683 NM_001126118.1:c.390G>C CA397841691 NM_001126118.1:c.390G>A CA397841695 NM_001126118.1:c.390G>T