Canonical Allele Identifier: PA2826564795
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1721838
ClinVar RCV Id: RCV002305383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Pro8Ala
CA397846769
NM_001276760.3:c.22C>G