Canonical Allele Identifier: PA2825607688
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376607
ClinVar Variation Id: 406578

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.His179Gln
CA16603028
NM_001126114.3:c.537T>G
CA16615708
NM_001126114.3:c.537T>A