ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579934306
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
376582
ClinVar RCV Id:
RCV000418840
RCV000420903
RCV000423743
RCV000423016
RCV000425095
RCV000429558
RCV000428868
RCV000430324
RCV000431612
RCV000434455
RCV000432328
RCV000436058
RCV000440235
RCV000441009
RCV000441652
RCV000442601
RCV000785323
RCV001861482
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Cys275Phe
CA16603006
NM_000546.6:c.824G>T