ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825618054
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
376650
ClinVar RCV Id:
RCV000417467
RCV000418814
RCV000418608
RCV000421737
RCV000422458
RCV000422684
RCV000428488
RCV000428624
RCV000428841
RCV000427240
RCV000427500
RCV000433789
RCV000432738
RCV000435387
RCV000435132
RCV000437481
RCV000438469
RCV000439587
RCV000439979
RCV000443648
RCV000444469
RCV000445195
RCV001371092
RCV004022236
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119590.1:p.Arg174Leu
CA16603067
NM_001126118.1:c.521G>T