Canonical Allele Identifier: PA2826565999
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376657
ClinVar RCV Id: RCV000418023 RCV000425366 RCV000423448 RCV000423739 RCV000423933 RCV000428952 RCV000428734 RCV000431165 RCV000433592 RCV000433708 RCV000436148 RCV000436528 RCV000438568 RCV000440980 RCV000442077 RCV000444685 RCV000444610 RCV000492483 RCV000633356
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Arg241Lys
CA16603072
NM_001276760.3:c.722G>A