Canonical Allele Identifier: PA2825615688
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376654
ClinVar RCV Id: RCV000418381 RCV000419254 RCV000421216 RCV000423993 RCV000427287 RCV000426656 RCV000427933 RCV000428633 RCV000429532 RCV000436273 RCV000436898 RCV000438863 RCV000437517 RCV000441694 RCV000444068 RCV000467567 RCV000581522 RCV000785305 RCV001026460 RCV002289533
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Arg117Gly
CA16603071
NM_001126117.1:c.349A>G