Canonical Allele Identifier: PA190295
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 184863

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Ala6Val
CA000168
NM_001126116.1:c.17C>T
CA645589163
NM_001126116.1:c.17_18delinsTT