Canonical Allele Identifier: PA261560
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40487
ClinVar RCV Id: RCV000033455 RCV000037627 RCV000234028 RCV000768061 RCV001283812 RCV002408493 RCV001813242 RCV003333002 RCV003991571 RCV003333001 RCV004532483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Asn58Asp
CA261558
NM_002834.5:c.172A>G