Canonical Allele Identifier: PA2825605004
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376638
ClinVar RCV Id: RCV000420547 RCV000417510 RCV000418162 RCV000424579 RCV000425771 RCV000430564 RCV000436479 RCV000435297 RCV000431205 RCV000441278 RCV000442232 RCV000633336 RCV002374626
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119585.1:p.Asn239Thr
CA16603055
NM_001126113.3:c.716A>C