Canonical Allele Identifier: PA2826561820
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 924895
ClinVar RCV Id: RCV001186550
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Thr295Ile
CA397835429
NM_001276696.3:c.884C>T