Canonical Allele Identifier: PA1139678555
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 924379
ClinVar RCV Id: RCV001185668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Asn68Ser
CA397840455
NM_001126117.1:c.203A>G