Canonical Allele Identifier: PA2828530601
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40528
ClinVar RCV Id: RCV000037662 RCV000077861 RCV000231840 RCV000586058 RCV000762885 RCV000856809 RCV002288529 RCV004018710 RCV004532490
ClinVar Variation Id: 44615
ClinVar RCV Id: RCV000037665 RCV000159052 RCV000587757 RCV000687570 RCV002288537
ClinVar Variation Id: 1201246
ClinVar RCV Id: RCV001566530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361554.1:p.Phe284Leu
CA220155
NM_001374625.1:c.850T>C
CA261606
NM_001374625.1:c.852T>G
CA386790412
NM_001374625.1:c.852T>A