Canonical Allele Identifier: PA916056461
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 13339
ClinVar RCV Id: RCV000014267 RCV000033477 RCV000424761 RCV000424995 RCV000432192 RCV000443046 RCV000444034
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Glu76Ala
CA123047
NM_080601.3:c.227A>C