Canonical Allele Identifier: PA156338
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 132973
ClinVar RCV Id: RCV000119375 RCV000486480 RCV000633378 RCV000774785 RCV003987365
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.His296Tyr
CA000474
NM_001126112.3:c.886C>T