Canonical Allele Identifier: PA916056406
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40487
ClinVar RCV Id: RCV000033455 RCV000037627 RCV000234028 RCV000768061 RCV001283812 RCV002408493 RCV001813242 RCV003333002 RCV003991571 RCV003333001 RCV004532483
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Asn58Asp
CA261558
NM_080601.3:c.172A>G