Canonical Allele Identifier: PA2826562018
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Ile36Ser
CA16603039
NM_001276697.3:c.107T>G