Canonical Allele Identifier: PA2826563586
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Arg114Ser
CA001542
NM_001276698.3:c.340C>A
CA645588417
NM_001276698.3:c.340_342delinsTCG
CA645588420
NM_001276698.3:c.339_340delinsAA