ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579953857
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
575773
ClinVar RCV Id:
RCV000698086
RCV001183319
RCV002289975
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Ala69Thr
CA397845904
NM_000546.6:c.205G>A