Canonical Allele Identifier: PA2826562277
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376578
ClinVar RCV Id: RCV000417879 RCV000418512 RCV000424746 RCV000425032 RCV000427153 RCV000433671 RCV000435743 RCV000435022 RCV000438269 RCV000442305 RCV000442449 RCV000688366 RCV000785473 RCV002379285
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Cys83Phe
CA501203
NM_001276697.3:c.248G>T
CA645588597
NM_001276697.3:c.248_249delinsTT