Canonical Allele Identifier: PA2825619404
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_001119590.1:p.His329Gln
CA397830872
NM_001126118.1:c.987C>G
CA397830875
NM_001126118.1:c.987C>A