Canonical Allele Identifier: PA2826562976
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 428899
ClinVar RCV Id: RCV000492698
ClinVar Variation Id: 2848594
ClinVar RCV Id: RCV003623190

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Lys5Asn
CA397841873
NM_001276698.3:c.15G>T
CA397841890
NM_001276698.3:c.15G>C