Canonical Allele Identifier: PA2825612747
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 919322

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Met37Ile
CA397841683
NM_001126116.1:c.111G>C
CA397841691
NM_001126116.1:c.111G>A
CA397841695
NM_001126116.1:c.111G>T