Canonical Allele Identifier: PA645436152
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406583
ClinVar RCV Id: RCV000477631 RCV000759377 RCV002348300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Pro45Leu
CA16615728
NM_001126117.1:c.134C>T
CA645588942
NM_001126117.1:c.134_135delinsTT