Canonical Allele Identifier: PA2825605398
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376673
ClinVar RCV Id: RCV000424786 RCV000429369 RCV000434183 RCV000438331 RCV000440060 RCV000442953 RCV000444340 RCV001228585 RCV000421804 RCV004022247 RCV000422825 RCV000423493 RCV000427639 RCV000433521 RCV000442761
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119585.1:p.Val272Glu
CA16603087
NM_001126113.3:c.815T>A