Canonical Allele Identifier: PA112981
Gene: PTEN HGNC NCBI

Linked Data

ClinVar Variation Id: 7815
ClinVar RCV Id: RCV000008259 RCV000735267
ClinVar Variation Id: 569301
ClinVar RCV Id: RCV000689896 RCV002343451 RCV003453439
ClinVar Variation Id: 825458
ClinVar RCV Id: RCV001023564 RCV003455124 RCV003509648 RCV003478652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000305.3:p.Ser170Arg
CA000492
NM_000314.7:c.510T>A
CA377484273
NM_000314.7:c.508A>C
CA377484279
NM_000314.7:c.510T>G