Canonical Allele Identifier: PA300192
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 161397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Pro90Leu
CA000317
NM_001126116.1:c.269C>T
CA645588718
NM_001126116.1:c.268_269delinsTT