Canonical Allele Identifier: PA2826564489
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 141102
ClinVar RCV Id: RCV000129462 RCV000204899 RCV000213063 RCV000411116 RCV001260345 RCV003935214
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Thr153Ser
CA000505
NM_001276699.3:c.458C>G
CA397836079
NM_001276699.3:c.457A>T