Canonical Allele Identifier: PA645435679
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376574
ClinVar RCV Id: RCV000418555 RCV000417498 RCV000422481 RCV000422719 RCV000425072 RCV000427235 RCV000427531 RCV000428817 RCV000433989 RCV000432745 RCV000435343 RCV000433862 RCV000435149 RCV000439349 RCV000440369 RCV000442469 RCV000444988 RCV000473420 RCV002365459 RCV004022207
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Cys238Phe
CA16603000
NM_001126114.3:c.713G>T