Canonical Allele Identifier: PA1139677589
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 935999
ClinVar RCV Id: RCV001204709 RCV002436787
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Pro34Ser
CA397848062
NM_001126114.3:c.100C>T