Canonical Allele Identifier: PA2827312840
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2025797
ClinVar RCV Id: RCV002853422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Gln79His
CA6798533
NM_001330437.2:c.237G>C
CA386777930
NM_001330437.2:c.237G>T