Canonical Allele Identifier: PA2825612130
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 858737
ClinVar RCV Id: RCV001064680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Ser235Thr
CA397831738
NM_001126115.1:c.704G>C