Canonical Allele Identifier: PA916006477
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 659842
ClinVar RCV Id: RCV000816907 RCV002381838
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Leu6Val
CA397846833
NM_001276761.3:c.16C>G