Canonical Allele Identifier: PA273469
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 177791
ClinVar RCV Id: RCV000154419 RCV000236210 RCV000426195 RCV000429339 RCV000438488 RCV000439590 RCV000442616 RCV000417965 RCV000420364 RCV000425780 RCV000426900 RCV000428236 RCV000432564 RCV000438178 RCV000439098 RCV000442642 RCV000422573 RCV000419417 RCV000430604 RCV000431373 RCV000437089 RCV000492778 RCV000785321 RCV002288664
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Ser109Cys
CA000357
NM_001126117.1:c.326C>G