Canonical Allele Identifier: PA2826562869
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 485038
ClinVar Variation Id: 657014

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.His209Gln
CA397830872
NM_001276697.3:c.627C>G
CA397830875
NM_001276697.3:c.627C>A