Canonical Allele Identifier: PA645436284
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 265337
ClinVar RCV Id: RCV000255449 RCV000418361 RCV000427564 RCV000437324 RCV000439730 RCV000445278 RCV000429054 RCV000430142 RCV000436667 RCV000419408 RCV000700891 RCV000772138 RCV000785239 RCV002282093 RCV004021028
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Ser83Gly
CA10588671
NM_001126117.1:c.247A>G