Canonical Allele Identifier: PA2825619215
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2585878
ClinVar RCV Id: RCV003341665
ClinVar Variation Id: 3071734
ClinVar RCV Id: RCV004016228 RCV004371957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Phe302Leu
CA397832608
NM_001126118.1:c.906C>A
CA397832612
NM_001126118.1:c.906C>G
CA397832628
NM_001126118.1:c.904T>C