Canonical Allele Identifier: PA2825616476
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 492650

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Ser214Leu
CA000974
NM_001126117.1:c.641C>T