Canonical Allele Identifier: PA190369
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 184882
ClinVar RCV Id: RCV000164218 RCV000785503 RCV001338713
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119585.1:p.Asn247Ile
CA000378
NM_001126113.3:c.740A>T
CA645588553
NM_001126113.3:c.740_741delinsTA