Canonical Allele Identifier: PA2826560682
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 419837
ClinVar RCV Id: RCV000484765 RCV000526166 RCV000569220 RCV001724024
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Thr79Ile
CA16620635
NM_001276696.3:c.236C>T