Canonical Allele Identifier: PA2579951407
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2585878
ClinVar RCV Id: RCV003341665
ClinVar Variation Id: 3071734

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Phe341Leu
CA397832608
NM_000546.6:c.1023C>A
CA397832612
NM_000546.6:c.1023C>G
CA397832628
NM_000546.6:c.1021T>C