Canonical Allele Identifier: PA2825618656
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 233303
ClinVar RCV Id: RCV000220597 RCV000422798 RCV000422392 RCV000427379 RCV000428065 RCV000424659 RCV000429134 RCV000433685 RCV000434748 RCV000435298 RCV000439374 RCV000437591 RCV000444359 RCV000440058 RCV000417840 RCV000434911 RCV000423426 RCV000444283 RCV000445304 RCV001854689 RCV002288888
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Gly227Val
CA10580919
NM_001126118.1:c.680G>T