Canonical Allele Identifier: PA2826561379
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376600
ClinVar RCV Id: RCV000418805 RCV000421362 RCV000425382 RCV000423748 RCV000426057 RCV000426513 RCV000432031 RCV000433704 RCV000436060 RCV000434459 RCV000441006 RCV000442909 RCV000443654 RCV000492366 RCV000633372 RCV001257520 RCV002289524 RCV003168616 RCV003476007 RCV003332172
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Gly205Ser
CA16603022
NM_001276696.3:c.613G>A