Canonical Allele Identifier: PA2826567091
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1019369
ClinVar RCV Id: RCV001318797
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Thr172Ser
CA397840130
NM_001276761.3:c.515C>G
CA397840132
NM_001276761.3:c.514A>T