Canonical Allele Identifier: PA2827312826
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 13338
ClinVar RCV Id: RCV000014266 RCV000159046 RCV000420699 RCV000437713 RCV000419574 RCV000427060 RCV000437931 RCV002513040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Glu76Gly
CA123044
NM_001330437.2:c.227A>G