Canonical Allele Identifier: PA658664701
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 480737
ClinVar RCV Id: RCV000572422 RCV003767116
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Thr84Ile
CA397844286
NM_001126118.1:c.251C>T