Canonical Allele Identifier: PA2827312757
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 228392
ClinVar RCV Id: RCV000215649 RCV001090939 RCV003992237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Asp61Tyr
CA10576907
NM_001330437.2:c.181G>T
CA243707918
NM_001330437.2:c.180_181delinsGT