Canonical Allele Identifier: PA645435422
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406604

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Pro13Ser
CA16616008
NM_001126114.3:c.37C>T