ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826560687
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
141098
ClinVar RCV Id:
RCV000129457
RCV000213049
RCV000696142
RCV000785522
RCV004019730
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263625.1:p.Lys81Glu
CA000130
NM_001276696.3:c.241A>G