Canonical Allele Identifier: PA2825614242
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1718571
ClinVar RCV Id: RCV002299896
ClinVar Variation Id: 2679235
ClinVar RCV Id: RCV003464702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Lys160Asn
CA397836532
NM_001126116.1:c.480A>T
CA397836533
NM_001126116.1:c.480A>C