Canonical Allele Identifier: PA2827312771
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2756656
ClinVar RCV Id: RCV003540328

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Tyr62Ser
CA386777608
NM_001330437.2:c.185A>C