Canonical Allele Identifier: PA261593
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 44613
ClinVar RCV Id: RCV000037656 RCV000159049 RCV001002142
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Glu258Asp
CA261591
NM_002834.5:c.774G>T
CA386788489
NM_002834.5:c.774G>C