Canonical Allele Identifier: PA106972
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
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Gly244Asp
CA16043048
NM_000546.6:c.731G>A