Canonical Allele Identifier: PA2825602821
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1361888
ClinVar RCV Id: RCV001932008
ClinVar Variation Id: 1506044
ClinVar RCV Id: RCV001999673
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119585.1:p.Asp49Glu
CA397846609
NM_001126113.3:c.147T>A
CA397846612
NM_001126113.3:c.147T>G