Canonical Allele Identifier: PA190297
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 184863

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Ala99Val
CA000168
NM_001126118.1:c.296C>T
CA645589163
NM_001126118.1:c.296_297delinsTT