Canonical Allele Identifier: PA916006758
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376560
ClinVar RCV Id: RCV000418091 RCV000423943 RCV000422903 RCV000425388 RCV000426036 RCV000430504 RCV000433604 RCV000432610 RCV000434656 RCV000440105 RCV000441192 RCV000444209 RCV000444995 RCV001383908 RCV004022200
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Cys96Arg
CA16602986
NM_001276761.3:c.286T>C