Canonical Allele Identifier: PA282075
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40496
ClinVar RCV Id: RCV000687319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Asp61Val
CA282073
NM_002834.5:c.182A>T