ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826563015
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
428909
ClinVar RCV Id:
RCV000492688
RCV002527066
RCV004023284
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263627.1:p.Val13Phe
CA397841576
NM_001276698.3:c.37G>T