Canonical Allele Identifier: PA2825608149
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376671
ClinVar RCV Id: RCV000422282 RCV000423344 RCV000424582 RCV000427043 RCV000433620 RCV000433417 RCV000434681 RCV000439990 RCV000440155 RCV000442891 RCV000442920 RCV001202958
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Val216Gly
CA16603085
NM_001126114.3:c.647T>G