Canonical Allele Identifier: PA2826567480
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376582
ClinVar RCV Id: RCV000418840 RCV000420903 RCV000423743 RCV000423016 RCV000425095 RCV000429558 RCV000428868 RCV000430324 RCV000431612 RCV000434455 RCV000432328 RCV000436058 RCV000440235 RCV000441009 RCV000441652 RCV000442601 RCV000785323 RCV001861482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Cys236Phe
CA16603006
NM_001276761.3:c.707G>T