Canonical Allele Identifier: PA915980226
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 826488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Pro87Leu
CA397839907
NM_001126117.1:c.260C>T
CA645588728
NM_001126117.1:c.260_261delinsTT