Canonical Allele Identifier: PA2827312941
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1302952
ClinVar RCV Id: RCV001756451

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Gly154Ser
CA386781496
NM_001330437.2:c.460G>A