Canonical Allele Identifier: PA177667
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 13330
ClinVar RCV Id: RCV000014258 RCV000033464 RCV000077856 RCV000156984 RCV000626829 RCV000824738 RCV001270166 RCV001376030 RCV001813196 RCV002490363 RCV003147285 RCV004532341
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Asp61Gly
CA177665
NM_002834.5:c.182A>G