Canonical Allele Identifier: PA1139746059
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 981582
ClinVar RCV Id: RCV001261103
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Lys129Asn
CA386780893
NM_080601.3:c.387A>C
CA386780896
NM_080601.3:c.387A>T