Canonical Allele Identifier: PA916006347
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 372785
ClinVar RCV Id: RCV000413969 RCV000421269 RCV000422456 RCV000419371 RCV000423079 RCV000429659 RCV000428997 RCV000431939 RCV000432739 RCV000440742 RCV000439239 RCV000427142 RCV000444224 RCV000561866 RCV000444195 RCV000477083 RCV000785537 RCV002288986 RCV003168599
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Gly85Asp
CA16043048
NM_001276699.3:c.254G>A