Canonical Allele Identifier: PA194089
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 186179
ClinVar RCV Id: RCV000165724 RCV000986051 RCV000804037 RCV001192618
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Thr23Ser
CA000210
NM_001126116.1:c.68C>G
CA397842094
NM_001126116.1:c.67A>T