Canonical Allele Identifier: PA2826563852
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 492635
ClinVar RCV Id: RCV000583939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Gln174Glu
CA001088
NM_001276698.3:c.520C>G