Canonical Allele Identifier: PA2826567784
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 43587
ClinVar RCV Id: RCV000036529 RCV000492626 RCV000255021 RCV000468537 RCV003315555
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Ala308Asp
CA000022
NM_001276761.3:c.923C>A