Canonical Allele Identifier: PA2825612139
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 485038
ClinVar RCV Id: RCV000575539 RCV000798387 RCV002289832
ClinVar Variation Id: 657014
ClinVar RCV Id: RCV000813556 RCV001009899 RCV002290459
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.His236Gln
CA397830872
NM_001126115.1:c.708C>G
CA397830875
NM_001126115.1:c.708C>A