Canonical Allele Identifier: PA2826567869
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 188342

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.His329Tyr
CA000039
NM_001276761.3:c.985C>T