Canonical Allele Identifier: PA2825613640
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376602
ClinVar RCV Id: RCV000419267 RCV000420351 RCV000418001 RCV000424520 RCV000425133 RCV000425485 RCV000430145 RCV000431028 RCV000432729 RCV000435229 RCV000437599 RCV000438254 RCV000443153
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Gly112Arg
CA16603024
NM_001126116.1:c.334G>C