Canonical Allele Identifier: PA2825603353
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1460570
ClinVar RCV Id: RCV001951660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119585.1:p.Thr123Ser
CA397844287
NM_001126113.3:c.368C>G
CA397844300
NM_001126113.3:c.367A>T