Canonical Allele Identifier: PA2826563700
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1338368
ClinVar RCV Id: RCV001817739

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Arg131Ser
CA397836603
NM_001276698.3:c.391C>A
CA2573054585
NM_001276698.3:c.390_391delinsAA