Canonical Allele Identifier: PA168940
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142624

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Arg49Cys
CA000257
NM_001126117.1:c.145C>T
CA645588898
NM_001126117.1:c.145_150delinsTGCTGT