ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA300206
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
182934
ClinVar RCV Id:
RCV000161033
RCV000200500
RCV000421083
RCV000421733
RCV000430423
RCV000431774
RCV000439317
RCV000439996
RCV000419726
RCV000422107
RCV000429307
RCV000434187
RCV000443583
RCV000443569
RCV001526334
RCV002288692
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119584.1:p.Met237Val
CA000348
NM_001126112.3:c.709A>G