ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA164820
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
80708
ClinVar RCV Id:
RCV000129635
RCV000701624
RCV001127281
RCV001358057
RCV003894916
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.His365Tyr
CA000035
NM_000546.6:c.1093C>T