Allele Registry

Canonical Allele Identifier: PA916056524

Gene: PTPN11 HGNC NCBI

ClinVar Allele:

48988

ClinVar RCV:

RCV000033497

RCV000157681

RCV000506790

RCV000585640

RCV000824743

RCV002399353

ClinVar Variation:

40518

HGVS (amino-acid)	Matching Registered Transcripts
NP_542168.1:p.Gln256Arg	CA235325 NM_080601.3:c.767A>G