Canonical Allele Identifier: PA191628
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 185319
ClinVar RCV Id: RCV000164718 RCV003765021
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Ala237Gly
CA000436
NM_001126118.1:c.710C>G