Canonical Allele Identifier: PA2826559598
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 141359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Ser146Asn
CA000264
NM_001276695.3:c.437G>A