Canonical Allele Identifier: PA2742003780
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2735977
ClinVar RCV Id: RCV003540157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Gln79Pro
CA386777926
NM_080601.3:c.236A>C