Canonical Allele Identifier: PA2826565700
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 127821

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Asn196Ser
CA000343
NM_001276760.3:c.587A>G