Canonical Allele Identifier: PA2826566552
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 836766
ClinVar RCV Id: RCV001037964
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Pro36Leu
CA397845650
NM_001276761.3:c.107C>T