Canonical Allele Identifier: PA2826563941
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376607
ClinVar Variation Id: 406578

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.His20Gln
CA16603028
NM_001276699.3:c.60T>G
CA16615708
NM_001276699.3:c.60T>A