Canonical Allele Identifier: PA2825613799
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376623
ClinVar RCV Id: RCV000420356 RCV000420641 RCV000424525 RCV000427837 RCV000435232 RCV000437646 RCV000442535 RCV000458707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Ile123Thr
CA16603043
NM_001126116.1:c.368T>C