Canonical Allele Identifier: PA916056637
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40541
ClinVar RCV Id: RCV000373942 RCV000521244 RCV001582506 RCV002399354 RCV003315540 RCV004541059
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Arg351Gln
CA282114
NM_080601.3:c.1052G>A