Canonical Allele Identifier: PA2825618347
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376638
ClinVar RCV Id: RCV000420547 RCV000417510 RCV000418162 RCV000424579 RCV000425771 RCV000430564 RCV000436479 RCV000435297 RCV000431205 RCV000441278 RCV000442232 RCV000633336 RCV002374626
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Asn200Thr
CA16603055
NM_001126118.1:c.599A>C