Canonical Allele Identifier: PA2825618042
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1019369
ClinVar RCV Id: RCV001318797

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Thr172Ser
CA397840130
NM_001126118.1:c.515C>G
CA397840132
NM_001126118.1:c.514A>T