Canonical Allele Identifier: PA2826567675
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406585

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Gln278His
CA16615689
NM_001276761.3:c.834G>T
CA397835964
NM_001276761.3:c.834G>C