Canonical Allele Identifier: PA916006438
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376622
ClinVar RCV Id: RCV000417507 RCV000420747 RCV000423148 RCV000428170 RCV000430544 RCV000441277 RCV000441504 RCV001225201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Ile96Ser
CA16603042
NM_001276699.3:c.287T>G