Canonical Allele Identifier: PA916028157
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40560
ClinVar RCV Id: RCV000419381 RCV000430281 RCV000429259 RCV000439943 RCV000440091 RCV000505671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Gly507Val
CA282129
NM_001330437.2:c.1520G>T