Canonical Allele Identifier: PA2826567114
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376660
ClinVar RCV Id: RCV000420217 RCV000420881 RCV000423272 RCV000429840 RCV000430889 RCV000433950 RCV000435696 RCV000441630 RCV000440493 RCV000785347 RCV001025280 RCV003509529
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Ser176Ile
CA16603075
NM_001276761.3:c.527G>T