ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826563014
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
836761
ClinVar RCV Id:
RCV001037957
RCV002337102
RCV003396634
RCV004031050
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263627.1:p.Val13Asp
CA397841557
NM_001276698.3:c.38T>A