Canonical Allele Identifier: PA2826564868
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 490170

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Glu29Gln
CA397845956
NM_001276760.3:c.85G>C