ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579951860
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
528273
ClinVar RCV Id:
RCV000633395
RCV001019395
RCV002289935
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Pro316Leu
CA397835981
NM_000546.6:c.947C>T