Canonical Allele Identifier: PA2826563180
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 482218
ClinVar Variation Id: 482235

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Val44Leu
CA397840385
NM_001276698.3:c.130G>T
CA397840390
NM_001276698.3:c.130G>C