Canonical Allele Identifier: PA2826563871
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 919322

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Met10Ile
CA397841683
NM_001276699.3:c.30G>C
CA397841691
NM_001276699.3:c.30G>A
CA397841695
NM_001276699.3:c.30G>T