Canonical Allele Identifier: PA190291
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 184863
ClinVar RCV Id: RCV000164195 RCV000813957 RCV003474852 RCV003995323 RCV004019963
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Ala138Val
CA000168
NM_001126112.3:c.413C>T
CA645589163
NM_001126112.3:c.413_414delinsTT