Canonical Allele Identifier: PA1139677333
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 927316
ClinVar RCV Id: RCV001190530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Ser366Cys
CA397831748
NM_001126112.3:c.1097C>G