Canonical Allele Identifier: PA106980
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376601
ClinVar RCV Id: RCV000417831 RCV000420188 RCV000423073 RCV000424338 RCV000428522 RCV000430897 RCV000433321 RCV000433805 RCV000434977 RCV000440310 RCV000439173 RCV000441607 RCV000443964 RCV000785338 RCV004022214
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Gly244Val
CA16603023
NM_000546.6:c.731G>T