Canonical Allele Identifier: PA916056398
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 477669
ClinVar RCV Id: RCV000531774 RCV000788007
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Ile56Thr
CA243707917
NM_080601.3:c.167T>C