ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826563196
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
439319
ClinVar RCV Id:
RCV000507226
RCV000566251
RCV001049540
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263627.1:p.Leu47Ser
CA397840264
NM_001276698.3:c.140T>C