Canonical Allele Identifier: PA2825611502
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1338368
ClinVar RCV Id: RCV001817739

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Arg158Ser
CA397836603
NM_001126115.1:c.472C>A
CA2573054585
NM_001126115.1:c.471_472delinsAA