Canonical Allele Identifier: PA2826566474
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2130489
ClinVar RCV Id: RCV003052105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Thr16Ser
CA397846406
NM_001276761.3:c.47C>G
CA397846418
NM_001276761.3:c.46A>T