ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826559203
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
141302
ClinVar RCV Id:
RCV000129770
RCV000633376
RCV002288629
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263624.1:p.Phe74Val
CA000124
NM_001276695.3:c.220T>G