ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579935272
Gene: TP53
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000417799
RCV000418899
RCV000421946
RCV000422882
RCV000423390
RCV000425213
RCV000427437
RCV000428035
RCV000429092
RCV000430183
RCV000433139
RCV000433946
RCV000435497
RCV000436563
RCV000437871
RCV000439326
RCV000442103
RCV000442139
RCV000443312
RCV000785263
RCV001057485
ClinVar Variation:
376664
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Ser241Pro
CA16603079
NM_000546.6:c.721T>C