Canonical Allele Identifier: PA645436038
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376567
ClinVar RCV Id: RCV000417913 RCV000420314 RCV000422574 RCV000421892 RCV000428237 RCV000430556 RCV000432852 RCV000433900 RCV000438490 RCV000439057 RCV000439533 RCV000442038
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Cys9Ser
CA16602993
NM_001126117.1:c.25T>A
CA397842593
NM_001126117.1:c.26G>C