Canonical Allele Identifier: PA2825618587
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2671888
ClinVar RCV Id: RCV003449010
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Asp220Ala
CA397837636
NM_001126118.1:c.659A>C