Canonical Allele Identifier: PA2826567277
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_001263690.1:p.Cys203Ser
CA001776
NM_001276761.3:c.608G>C
CA16603004
NM_001276761.3:c.607T>A
CA2580094896
NM_001276761.3:c.608_609delinsCA