Canonical Allele Identifier: PA645436028
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376566
ClinVar RCV Id: RCV000419137 RCV000420961 RCV000425541 RCV000426677 RCV000427661 RCV000432339 RCV000432969 RCV000436820 RCV000437911 RCV000438636 RCV000444521 RCV000444835
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Cys9Gly
CA16602992
NM_001126117.1:c.25T>G