Canonical Allele Identifier: PA2827312912
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_001317366.1:p.Lys129Asn
CA386780893
NM_001330437.2:c.387A>C
CA386780896
NM_001330437.2:c.387A>T