Canonical Allele Identifier: PA2826559479
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 127814
ClinVar RCV Id: RCV000115725 RCV000419946 RCV000436926 RCV000419252 RCV000430191 RCV000434251 RCV000442798 RCV000427698 RCV000434917 RCV000443742 RCV000526324 RCV000423543 RCV000424864 RCV000429510 RCV000785334 RCV000435593 RCV000443833 RCV000492788 RCV004019613
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Tyr124Cys
CA000240
NM_001276695.3:c.371A>G