Canonical Allele Identifier: PA916056495
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 409673
ClinVar RCV Id: RCV000472224
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Ser140Cys
CA16613668
NM_080601.3:c.418A>T