ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA174234
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
161517
ClinVar RCV Id:
RCV000149052
RCV000417523
RCV000426315
RCV000428657
RCV000435871
RCV000437418
RCV000438665
RCV000438915
RCV000442289
RCV000445006
RCV000421544
RCV000434213
RCV000419067
RCV000419744
RCV000425612
RCV000427666
RCV000429336
RCV000434436
RCV000633330
RCV004019784
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119588.1:p.Arg148Ile
CA000447
NM_001126116.1:c.443G>T