Canonical Allele Identifier: PA2826562811
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1778759
ClinVar RCV Id: RCV002399057
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Asp193Glu
CA397832224
NM_001276697.3:c.579T>A
CA397832227
NM_001276697.3:c.579T>G