Canonical Allele Identifier: PA1139677338
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 858737
ClinVar RCV Id: RCV001064680

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Ser367Thr
CA397831738
NM_001126112.3:c.1100G>C