Canonical Allele Identifier: PA2825616850
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 821636
ClinVar RCV Id: RCV001016237

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Pro50Thr
CA397845257
NM_001126118.1:c.148C>A