Canonical Allele Identifier: PA2826563768
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1471105
ClinVar RCV Id: RCV001995379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Pro150Leu
CA397836130
NM_001276698.3:c.449C>T