Canonical Allele Identifier: PA2825605657
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1495821
ClinVar RCV Id: RCV001991580

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119585.1:p.Glu298Gln
CA397836431
NM_001126113.3:c.892G>C