Canonical Allele Identifier: PA2825618989
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1469089
ClinVar RCV Id: RCV001993812

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Pro262Ser
CA397836354
NM_001126118.1:c.784C>T