Canonical Allele Identifier: PA2825616766
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406593

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Pro41Ser
CA16615999
NM_001126118.1:c.121C>T