Canonical Allele Identifier: PA645436314
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376689
ClinVar RCV Id: RCV000417982 RCV000418575 RCV000418779 RCV000422783 RCV000427506 RCV000426793 RCV000428144 RCV000431034 RCV000430837 RCV000433449 RCV000434918 RCV000436457 RCV000437034 RCV000441127 RCV000440413 RCV000444915 RCV000444073 RCV001851023 RCV000424311 RCV000425315 RCV004022255
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Tyr88Asp
CA16603102
NM_001126117.1:c.262T>G