Canonical Allele Identifier: PA916056465
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 13337
ClinVar RCV Id: RCV000014265 RCV000781775 RCV000788241 RCV001813201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Glu76Val
CA123041
NM_080601.3:c.227A>T