Canonical Allele Identifier: PA2826563691
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 822635

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Leu130Phe
CA397836616
NM_001276698.3:c.388C>T