Canonical Allele Identifier: PA2825611707
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 927085
ClinVar RCV Id: RCV001190099

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Ser183Cys
CA397836006
NM_001126115.1:c.548C>G