Canonical Allele Identifier: PA2826563395
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376579
ClinVar Variation Id: 647334
ClinVar Variation Id: 2124706
ClinVar RCV Id: RCV003039749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Cys83Ser
CA001776
NM_001276698.3:c.248G>C
CA16603004
NM_001276698.3:c.247T>A
CA2580094896
NM_001276698.3:c.248_249delinsCA