Canonical Allele Identifier: PA2825618898
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1024822
ClinVar RCV Id: RCV001325049

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Asn249Asp
CA397836643
NM_001126118.1:c.745A>G