Canonical Allele Identifier: PA203422
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12356

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Arg116Gln
CA000387
NM_001126115.1:c.347G>A
CA645588545
NM_001126115.1:c.347_348delinsAA