Canonical Allele Identifier: PA645438177
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 428902

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Asn92Ile
CA397842926
NM_001126118.1:c.275A>T