Canonical Allele Identifier: PA2825619197
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 482226
ClinVar RCV Id: RCV000576115 RCV001322989 RCV002289821
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Phe299Leu
CA000848
NM_001126118.1:c.897C>G
CA397832711
NM_001126118.1:c.897C>A
CA397832735
NM_001126118.1:c.895T>C