Canonical Allele Identifier: PA2827313183
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 620593
ClinVar RCV Id: RCV000761000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Phe314Leu
CA243712000
NM_001330437.2:c.940T>C
CA386791017
NM_001330437.2:c.942T>A
CA386791020
NM_001330437.2:c.942T>G