Canonical Allele Identifier: PA916056578
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 44616
ClinVar RCV Id: RCV000037666
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Asp286Glu
CA134683
NM_080601.3:c.858T>A
CA386790433
NM_080601.3:c.858T>G