ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2825615740
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
376622
ClinVar RCV Id:
RCV000417507
RCV000420747
RCV000423148
RCV000428170
RCV000430544
RCV000441277
RCV000441504
RCV001225201
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119589.1:p.Ile123Ser
CA16603042
NM_001126117.1:c.368T>G