Canonical Allele Identifier: PA2579950874
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 485038
ClinVar Variation Id: 657014

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.His368Gln
CA397830872
NM_000546.6:c.1104C>G
CA397830875
NM_000546.6:c.1104C>A