Canonical Allele Identifier: PA916028158
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40562
ClinVar RCV Id: RCV000033549 RCV000077853 RCV000156983 RCV000677652 RCV000762887 RCV001027841 RCV002390132 RCV003991572 RCV004532496
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Met508Val
CA220140
NM_001330437.2:c.1522A>G