Canonical Allele Identifier: PA287699
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 127812
ClinVar RCV Id: RCV000115723 RCV000533951 RCV000508084 RCV001255633 RCV003483477 RCV002288596
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Arg26Cys
CA000225
NM_001126115.1:c.76C>T
CA645589032
NM_001126115.1:c.76_78delinsTGT
CA645589042
NM_001126115.1:c.75_76delinsTT