ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579936915
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
376630
ClinVar RCV Id:
RCV000417617
RCV000425579
RCV000425862
RCV000428739
RCV000435274
RCV000435918
RCV000441916
RCV000442239
RCV000459042
RCV000480700
RCV000785496
RCV004022227
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Leu111Pro
CA16603049
NM_000546.6:c.332T>C