Canonical Allele Identifier: PA2825609959
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2446885
ClinVar RCV Id: RCV003159585

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Glu39Asp
CA397841579
NM_001126115.1:c.117G>T
CA397841581
NM_001126115.1:c.117G>C