Canonical Allele Identifier: PA2826560675
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 649358
ClinVar RCV Id: RCV000804275 RCV002290445 RCV001020381 RCV003478506
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Ser77Ala
CA287488988
NM_001276696.3:c.229T>G