Canonical Allele Identifier: PA2826562335
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 420136
ClinVar RCV Id: RCV000479937 RCV000547538 RCV001026502
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Pro91Leu
CA16620620
NM_001276697.3:c.272C>T
CA645588533
NM_001276697.3:c.272_273delinsTT
CA645588536
NM_001276697.3:c.272_273delinsTG