Canonical Allele Identifier: PA916056586
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 181500
ClinVar RCV Id: RCV000159053 RCV000208167 RCV001850234 RCV001844054 RCV002372037 RCV002492630
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Asn298Ser
CA297088
NM_080601.3:c.893A>G