Canonical Allele Identifier: PA2826566886
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2446885
ClinVar RCV Id: RCV003159585
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Glu132Asp
CA397841579
NM_001276761.3:c.396G>T
CA397841581
NM_001276761.3:c.396G>C