Canonical Allele Identifier: PA2827312738
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40493
ClinVar RCV Id: RCV000037631 RCV000033461 RCV000416546 RCV000459297 RCV001813244 RCV002408494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Gly60Ala
CA261562
NM_001330437.2:c.179G>C