Canonical Allele Identifier: PA2826565997
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 161517
ClinVar RCV Id: RCV000149052 RCV000417523 RCV000426315 RCV000428657 RCV000435871 RCV000437418 RCV000438665 RCV000438915 RCV000442289 RCV000445006 RCV000421544 RCV000434213 RCV000419067 RCV000419744 RCV000425612 RCV000427666 RCV000429336 RCV000434436 RCV000633330 RCV004019784
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Arg241Ile
CA000447
NM_001276760.3:c.722G>T