Canonical Allele Identifier: PA2826561669
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1338368
ClinVar RCV Id: RCV001817739

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Arg251Ser
CA397836603
NM_001276696.3:c.751C>A
CA2573054585
NM_001276696.3:c.750_751delinsAA