Canonical Allele Identifier: PA2826565597
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376662
ClinVar RCV Id: RCV000422423 RCV000421424 RCV000423774 RCV000427974 RCV000432107 RCV000434496 RCV000438643 RCV000442434 RCV000443221 RCV000492171 RCV000816006 RCV003476011 RCV004022241
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Ser176Asn
CA16603077
NM_001276760.3:c.527G>A